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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2087151Generated: October 30, 2026

Diethyl Ether → (+)-β-Amino-3,4-difluoro-α,α-dimethylbenzeneethanol

https://huagongshe.com/reaction/2087151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 2-aMino-2-(3,4-difluorophenyl)acetateHCID 22049608—
ReactantHCID 178418573HCID 178418573—
Product(+)-β-Amino-3,4-difluoro-α,α-dimethylbenzeneethanolHCID 1862322962%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a well-stirred solution of methyl 2-amino-2-(3,4-difluorophenyl)acetate (10.5 g, 52.19 mmol) in anhydrous ether (200 mL) at 0° C. a solution of methylmagnesium bromide (3 M, 87 mL, 261 mmol) in ether was added over 10 minutes. The reaction mixture was stirred at 0° C. for 2.5 h and allowed to warm to room temperature. After 12 h, the reaction mixture was carefully poured onto a mixture of ice (300 g) and saturated aqueous ammonium chloride (50 9). The ether layer was separated and the aqueous layer was extracted with more ether (4×200 mL). The combined extracts were dried with magnesium sulfate and the solvent evaporated. The crude product was purified by column chromatography on silica gel using chloroform/methanol/2M ammonia in methanol (1000:20:10, 1000:40:20, 1000:80:40) as the eluent to give the product as an oil (6.5 g, 62% yield) which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727264B1
Source datasetuspto-grants-2004_04
ORD IDord-46409637879847edbb63caef28e3db96
Source noteuspto-grants-2004_04