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HRID 82355作成日:2026年10月26日

Water → (Z)-methyl 2-(tert-butoxycarbonyl)-3-(4-chloro-3-fluorophenyl)acrylate

https://huagongshe.com/reaction/82355

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1,1,3,3-TetramethylguanidineHCID 66460—
反応物4-Chloro-3-FluorobenzaldehydeHCID 2724985—
反応物Methyl2-(tert-butoxycarbonyl)-2-(dimethoxyphosphoryl)acetateHCID 86599651—
溶媒DichloromethaneHCID 6344—
生成物(Z)-methyl 2-(tert-butoxycarbonyl)-3-(4-chloro-3-fluorophenyl)acrylateHCID 6661795071.1%

反応条件

温度0 °C

反応手順

1,1,3,3-Tetramethylguanidine (2.11 mL, 16.8 mmol) was added to a 0° C. solution of methyl 2-(tert-butoxycarbonyl)-2-(dimethoxyphosphoryl)-acetate (5.00 g, 16.8 mmol) in DCM (70 mL). The reaction mixture stirred at 0° C. for 30 minutes, then a solution of 4-chloro-3-fluorobenzaldehyde (2.67 g, 16.8 mmol) in DCM (10 mL) was added by syringe. The reaction mixture was stirred for 10 minutes and then warmed to room temperature with continued stirring for 1 hour. H2O was then added, and the mixture was extracted with DCM. The combined extracts were dried (Na2SO4), filtered, and concentrated. The resulting solids were recrystallized from IPA to give (Z)-methyl 2-(tert-butoxycarbonyl)-3-(4-chloro-3-fluorophenyl)acrylate (3.76 g, 67.8% yield) as a white powder (2 crops). LCMS (APCI−) m/z 328 [M−H]−.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846681B2
出典データセットuspto-grants-2014_09
ORD IDord-d870addbf84d4f418593ae6d602956dc
出典メモuspto-grants-2014_09