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ChemicalBook--->CAS DataBase List--->68432-92-8

68432-92-8

68432-92-8 Structure

68432-92-8 Structure
IdentificationBack Directory
[Name]

3-CYANOMETHYLBENZOIC ACID METHYL ESTER
[CAS]

68432-92-8
[Synonyms]

Methyl m-(cyanomethyl)benzoate
METHYL 3-(CYANOMETHYL) BENZOATE
3-CYANOMETHYLBENZOIC ACID METHYL ESTER
Benzoicacid, 3-(cyanomethyl)-, methyl ester
high quality 3-CYANOMETHYLBENZOIC ACID METHYL ESTER
[Molecular Formula]

C10H9NO2
[MDL Number]

MFCD07783720
[MOL File]

68432-92-8.mol
[Molecular Weight]

175.18
Chemical PropertiesBack Directory
[Boiling point ]

314.1±25.0 °C(Predicted)
[density ]

1.141±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
[HazardClass ]

IRRITANT
[HS Code ]

2926907090
Hazard InformationBack Directory
[Uses]

Methyl 3-(cyanomethyl)benzoate is used as an intermediate in organic synthesis for the preparation of other compounds such as 3-(cyanomethyl)benzoic acid.
[Synthesis]

Methyl 3-(cyanomethyl)benzoate is synthesised using Methyl 3-(bromomethyl)benzoate as raw material by chemical reaction. The specific synthesis steps are as follows:
(i) To a solution of methyl 3-bromobenzoate (10.0 g, 44 mmol) in acetonitrile (100 mL) were added potassium cyanide (5.7 g, 87 mmol) and 18-crown-6 (1.0 g), and the mixture was stirred at room temperature for 3 days. The reaction mixture was filtered, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane=5/95-->30/70), and the fraction containing the object product was concentrated under reduced pressure to give the title compound (7.0 g, 91percent) as a colorless oil. 1H-NMR (DMSO-d6, 300 MHz) δ 3.88 (3H, s), 4.17 (2H, s), 7.57 (1H, t, J = 7.6 Hz), 7.61 - 7.69 (1H, m), 7.88 - 7.95 (1H, m), 7.97 (1H, br s).
Methyl 3-(cyanomethyl)benzoate synthesis
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