Anisole - Wikipedia

Organic compound (CH₃OC₆H₅) also named methoxybenzene Anisole

Names
Preferred IUPAC name Anisole[1]
Systematic IUPAC name Methoxybenzene[1]
Other names Methyl phenyl ether[1]Phenoxymethane
Identifiers
CAS Number	100-66-3 Y
3D model (JSmol)	Interactive image
Beilstein Reference	506892
ChEBI	CHEBI:16579 Y
ChEMBL	ChEMBL278024 Y
ChemSpider	7238 Y
ECHA InfoCard	100.002.615
EC Number	202-876-1
Gmelin Reference	2964
KEGG	C01403 Y
PubChem CID	7519
RTECS number	BZ8050000
UNII	B3W693GAZH Y
UN number	2222
CompTox Dashboard (EPA)	DTXSID4041608
InChI InChI=1S/C7H8O/c1-8-7-5-3-2-4-6-7/h2-6H,1H3 YKey: RDOXTESZEPMUJZ-UHFFFAOYSA-N Y InChI=1/C7H8O/c1-8-7-5-3-2-4-6-7/h2-6H,1H3Key: RDOXTESZEPMUJZ-UHFFFAOYAP
SMILES COc1ccccc1
Properties
Chemical formula	C7H8O
Molar mass	108.140 g·mol−1
Appearance	Colorless liquid
Density	0.995 g/cm3
Melting point	−37 °C (−35 °F; 236 K)
Boiling point	154 °C (309 °F; 427 K)
Solubility	Insoluble
Magnetic susceptibility (χ)	−72.79×10−6 cm3/mol
Hazards
GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H226, H315, H319
Precautionary statements	P210, P233, P240, P241, P242, P243, P264, P280, P302+P352, P303+P361+P353, P305+P351+P338, P321, P332+P313, P337+P313, P362, P370+P378, P403+P235, P501
NFPA 704 (fire diamond)	1 2 0
Lethal dose or concentration (LD, LC):
LD50 (median dose)	3700 mg/kg (rat, oral)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is YN ?) Infobox references

Chemical compound

Anisole, or methoxybenzene, is an organic compound with the formula CH3OC6H5. It is a colorless liquid with a smell reminiscent of anise seed, and in fact many of its derivatives are found in natural and artificial fragrances. The compound is mainly made synthetically and is a precursor to other synthetic compounds. Structurally, it is an ether (−O−) with a methyl (−CH3) and phenyl (−C6H5) group attached. Anisole is a standard reagent of both practical and pedagogical value.[2]

Reactivity

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Anisole undergoes electrophilic aromatic substitution reaction at a faster speed than benzene, which in turn reacts more quickly than nitrobenzene. The methoxy group is an ortho/para directing group, which means that electrophilic substitution preferentially occurs at these three sites. The enhanced nucleophilicity of anisole vs. benzene reflects the influence of the methoxy group, which renders the ring more electron-rich. The methoxy group strongly affects the pi cloud of the ring as a mesomeric electron donor, more so than as an inductive electron withdrawing group despite the electronegativity of the oxygen. Stated more quantitatively, the Hammett constant for para-substitution of anisole is –0.27.

Illustrative of its nucleophilicity, anisole reacts with acetic anhydride to give 4-methoxyacetophenone:

CH3OC6H5 + (CH3CO)2O → CH3OC6H4C(O)CH3 + CH3CO2H

Unlike most acetophenones, but reflecting the influence of the methoxy group, methoxyacetophenone undergoes a second acetylation. Many related reactions have been demonstrated. For example, phosphorus pentasulfide (P4S10) converts anisole to Lawesson's reagent, [(CH3OC6H4)PS2]2.[3]

Also indicating an electron-rich ring, anisole readily forms π-complexes with metal carbonyls, e.g. Cr(η6-anisole)(CO)3.[4]

The ether linkage is highly stable, but the methyl group can be removed with strong acids, such as hydroiodic acid or boron trichloride:[5]: 565–566 

CH3OC6H5 + HI → HOC6H5 + CH3I

Birch reduction of anisole gives 1-methoxycyclohexa-1,4-diene.[6]

Synthesis

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Anisole was first synthesized in 1841 by Auguste Cahours by barium anisate decarboxylation while heating p-anisic acid he made earlier from the anise essence with barium oxide:[7][8]

2 CH3OC6H4COOH + BaO → (CH3OC6H4COO)2Ba + H2O

(CH3OC6H4COO)2Ba → 2 CH3OC6H5 + BaCO3

It can be prepared by the Williamson ether synthesis from sodium phenoxide and dimethyl sulfate or methyl chloride:[9][5]

2 C6H5O− Na+ + (CH3O)2SO2 → 2 C6H5OCH3 + Na2SO4

Applications

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Anisole is a precursor to perfumes, insect pheromones, and pharmaceuticals.[5] For example, synthetic anethole is prepared from anisole.

Safety

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Anisole is relatively nontoxic with an LD50 of 3700 mg/kg in rats.[10] Its main hazard is its flammability.[10]

Popular culture

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In the board game Scrabble, the word "anisole" is the 39th-most-likely word (out of over 25,000 possibilities) for a "bingo"/"bonus", i.e. the deployment of all seven letters in one's own hand simultaneously.[11]

See also

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• Anethole
• Bromoanisole
• Butylated hydroxyanisole
• Ether
• Ethyl phenyl ether
• Phenol
• 2,4,6-Trichloroanisole (cork taint)

References

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1. ^ a b c Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. pp. 702–703. doi:10.1039/9781849733069-00648. ISBN 978-0-85404-182-4. Anisole, C6H5−O−CH3, is the only name in the class of ethers which is retained both as a preferred IUPAC name and for use in general nomenclature. For preferred IUPAC names, no substitution is allowed; for general nomenclature substitution is allowed on the ring and on the side chain under certain conditions (see P-34.1.1.4).
2. ^ Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, ISBN 978-0-471-72091-1
3. ^ I. Thomsen; K. Clausen; S. Scheibye; S.-O. Lawesson (1984). "Thiation with 2,4-Bis(4-Methoxyphenyl)-1,3,2,4-Dithiadiphosphetane 2,4-Disulfide: N-Methylthiopyrrolidone". Organic Syntheses. 62: 158. doi:10.15227/orgsyn.062.0158.
4. ^ E. Peter Kündig (2004). "Synthesis of Transition Metal η6-Arene Complexes". Topics Organomet Chem. Topics in Organometallic Chemistry. 7: 3–20. doi:10.1007/b94489. ISBN 978-3-540-01604-5.
5. ^ a b c Helmut Fiege; Heinz-Werner Voges; Toshikazu Hamamoto; Sumio Umemura; Tadao Iwata; Hisaya Miki; Yasuhiro Fujita; Hans-Josef Buysch; Dorothea Garbe; Wilfried Paulus. "Phenol Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_313. ISBN 978-3527306732.
6. ^ A. J. Birch and K. B. Chamberlain (1977). "Tricarbonyl[(2,3,4,5-η)-2,4-Cyclohexadien-1-one]Iron and Tricarbonyl[(1,2,3,4,5-η)-2-Methoxy-2,4-Cyclohexadien-1-yl]Iron(1+) Hexafluorophosphate(1−) from Anisole". Organic Syntheses. 57: 107. doi:10.15227/orgsyn.057.0107.
7. ^ Wisniak, Jaime (2013-10-01). "Auguste André Thomas Cahours". Educación Química. 24 (4): 451–460. doi:10.1016/S0187-893X(13)72500-X. ISSN 0187-893X.
8. ^ Crochard (París); Arago, François; Gay-Lussac, Joseph Louis (1841). Annales de chimie et de physique (in French). Chez Crochard.
9. ^ G. S. Hiers and F. D. Hager (1929). "Anisole". Organic Syntheses. 9: 12. doi:10.15227/orgsyn.009.0012.
10. ^ a b MSDS Archived July 1, 2010, at the Wayback Machine
11. ^ "Fun with analytics: Probabilities and Scrabble". www.illumine8.com. Retrieved 2023-12-08.

External links

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• International Chemical Safety Card 1014
• Pherobase pheromone database entry

Authority control databases: National	Germany