Methyl 4-(cyanomethyl)benzoate

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Methyl 4-(cyanomethyl)benzoate Basic information
Product Name:Methyl 4-(cyanomethyl)benzoate
Synonyms:4-CYANOMETHYLBENZOIC ACID METHYL ESTER;[p-(Methoxycarbonyl)phenyl]acetonitrile;Methyl p-(CyanoMethyl)benzoate;Methyl α-Cyano-p-toluate;α-Cyano-p-toluic Acid Methyl Ester;95.0%,(GC);METHYL 4-(CYANOMETHYL)BENZOATE;4-(Methoxycarbonyl)phenylacetonitrile, 4-(Methoxycarbonyl)benzyl cyanide
CAS:76469-88-0
MF:C10H9NO2
MW:175.18
EINECS:
Product Categories:Aromatic Esters;C10 to C11;Carbonyl Compounds;Esters;Aromatics;Intermediates;Intermediates & Fine Chemicals;Pharmaceuticals;Building Blocks;C10 to C11;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks
Mol File:76469-88-0.mol
Methyl 4-(cyanomethyl)benzoate Structure
Methyl 4-(cyanomethyl)benzoate Chemical Properties
Melting point 55-58 °C(lit.)
Boiling point 110 °C0.2 mm Hg(lit.)
density 1.141±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility soluble in Methanol
form powder to crystal
color White to Gray to Brown
InChIInChI=1S/C10H9NO2/c1-13-10(12)9-4-2-8(3-5-9)6-7-11/h2-5H,6H2,1H3
InChIKeyXRZGMNGGCZTNGE-UHFFFAOYSA-N
SMILESC(OC)(=O)C1=CC=C(CC#N)C=C1
CAS DataBase Reference76469-88-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HS Code 2926907090
Storage Class10 - Combustible liquids
Hazard ClassificationsAquatic Chronic 3
MSDS Information
ProviderLanguage
SigmaAldrich English
Methyl 4-(cyanomethyl)benzoate Usage And Synthesis
UsesThe key intermediate of Fexofenadine (F322490).
Synthesis
METHYL (4-HYDROXYMETHYL)BENZOATE

6908-41-4

POTASSIUM CYANIDE

151-50-8

Methyl 4-(cyanomethyl)benzoate

76469-88-0

Methyl 4-(hydroxymethyl)benzoate (1.00 g) was dissolved in dichloromethane (20 mL). To this solution was added triethylamine (0.9 mL), followed by the slow dropwise addition of a dichloromethane solution of methanesulfonyl chloride (0.70 g) (dichloromethane: 5 mL) under ice bath cooling. The reaction mixture was stirred for 15 h at room temperature, then diluted with dichloromethane, washed sequentially with water and dried with anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure and the resulting residue was dissolved in acetonitrile (12 mL). Potassium cyanide (0.80 g) and 18-crown-6 (0.16 g) were added and the mixture was stirred at room temperature for 40 hours. Upon completion of the reaction, the reaction mixture was concentrated under reduced pressure and the residue was diluted with dichloromethane, washed with water and dried over anhydrous sodium sulfate. The solvent was removed by distillation again under reduced pressure and the residue was purified by silica gel column chromatography (eluent: dichloromethane) to give a colorless crystalline product (0.91 g, 86% yield). A portion of the product was recrystallized from a solvent mixture of hexane and ethyl acetate to give colorless crystals. The product was characterized by 1H-NMR (CDCl3): δ 3.82 (2H, s), 3.93 (3H, s), 7.42 (2H, d, J = 8.3 Hz), 8.06 (2H, d, J = 8.3 Hz).

References[1] Patent: EP1577302, 2005, A1. Location in patent: Page/Page column 117
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