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HRID 81533作成日:2026年10月25日

Ethyl difluoroacetate → 1-(3-Bromophenyl)-2,2-difluoroethanone

https://huagongshe.com/reaction/81533

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl difluoroacetateHCID 9961—
反応物Benzene, 1-bromo-3-iodo-HCID 11561—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-(3-Bromophenyl)-2,2-difluoroethanoneHCID 86650253—

反応条件

温度-78 °C

反応手順

1-Bromo-3-iodo-benzene (22.5 g, 90 mmol, Aldrich) was dissolved in THF and cooled to −78° C. nBuLi (69.8 ml, 90 mmol) was added over 15 minutes and the reaction was stirred for 30 min. at −78° C. Difluoro-acetic acid ethyl ester (16.59 ml, 153 mmol, Aldrich) was added dropwise and stirring was continued for 3 hrs. After completion the reaction was quenched by the addition of 329 ml 2 M HCl solution and reaction was warmed to r.t. The phases were separated and the aqueous phases was extracted with Et2O. The organic phases were washed with water and brine, dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by automated column chromatography (cyclohexane/ethyl acetate) to yield the title compound as a yellow oil. 1H-NMR (360 MHz, DMSO-d6): 8.18 (s, 1H), 8.02 (m, 2H), 7.61 (t, 1H), 7.21 (t, 1H, CHF2); GC/MS: 234 [(M+H)+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846658B2
出典データセットuspto-grants-2014_09
ORD IDord-3718d39fb24641369c8a93360d8e97eb
出典メモuspto-grants-2014_09