ChemicalBook--->CAS DataBase List--->86239-00-1

86239-00-1

86239-00-1 Structure

86239-00-1 Structure
IdentificationBack Directory
[Name]

RARECHEM AL BI 0500
[CAS]

86239-00-1
[Synonyms]

RARECHEM AL BI 0500
Ethyl 3-fluoro-4-Methylbenzoate
3-FLUORO-4-METHYLBENZOIC ACID ETHYL ESTER
Benzoic acid, 3-fluoro-4-methyl-, ethyl ester
[Molecular Formula]

C10H11FO2
[MDL Number]

MFCD06204523
[MOL File]

86239-00-1.mol
[Molecular Weight]

182.19
Chemical PropertiesBack Directory
[Boiling point ]

240.8±28.0 °C(Predicted)
[density ]

1.108±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Light yellow to yellow Liquid
Safety DataBack Directory
[TSCA ]

TSCA listed
[HS Code ]

2916399090
Spectrum DetailBack Directory
[Spectrum Detail]

RARECHEM AL BI 0500(86239-00-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

Ethanol

64-17-5

3-Fluoro-4-methylbenzoic acid

350-28-7

RARECHEM AL BI 0500

86239-00-1

Thionyl chloride (3 mL) was added slowly and dropwise to a solution of 3-fluoro-4-methylbenzoic acid (13.23 g, 85.85 mmol) in anhydrous ethanol (200 mL) at 0 °C. The reaction mixture was warmed to 60 °C and stirred overnight. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently concentrated under reduced pressure. The concentrate was diluted with dichloromethane and the resulting organic phase was washed sequentially with 1N sodium hydroxide solution (100 mL x 2). The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give ethyl 3-fluoro-4-methylbenzoate (15.02 g, 96% yield).

[References]

[1] Patent: WO2011/71565, 2011, A1. Location in patent: Page/Page column 163
[2] Patent: WO2010/93845, 2010, A1. Location in patent: Page/Page column 153
[3] Journal of Medicinal Chemistry, 1983, vol. 26, # 9, p. 1282 - 1293
[4] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 5, p. 1421 - 1425
[5] Patent: WO2009/145360, 2009, A1. Location in patent: Page/Page column 129-130
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350-28-7