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HRID 449503作成日:2026年10月24日

3-Hydroxybenzaldehyde → Methyl 2-(tert-butoxycarbonylamino)-3-(3-hydroxyphenyl)acrylate

https://huagongshe.com/ja/reaction/449503

反応式

関与物質

役割名称HCID仕込み量
反応物3-HydroxybenzaldehydeHCID 101—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物Methyl ((tert-butoxy(hydroxy)methylidene)amino)(dimethoxyphosphoryl)acetateHCID 397380—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 2-(tert-butoxycarbonylamino)-3-(3-hydroxyphenyl)acrylateHCID 6754293696%

反応手順

Methyl [(tert-butoxycarbonyl)amino](dimethoxyphosphoryl)acetate (Fluka, Cat. #09659) (0.97 g, 3.3 mmol) and 3-hydroxybenzaldehyde (0.400 g, 3.28 mmol) were combined in methylene chloride (14 mL) at r.t. under nitrogen. To this DBU (0.68 mL, 3.9 mmol) was added and the reaction was stirred at r.t. for 2 h. The reaction was taken up in ethyl acetate, washed with 1 N HCl, brine, dried over magnesium sulfate and concentrated under reduced pressure to give the crude product as an oil. The product was purified by Flash chromatography on a silica gel column eluting hexane: ethyl acetate gradient to give methyl 2-(tert-butoxycarbonylamino)-3-(3-hydroxyphenyl)acrylate (0.92 g, 96%) as a clear oil Analytical LCMS (M+H-Boc)+: m/z=193.9.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481732B2
出典データセットuspto-grants-2013_07
ORD IDord-c0676be429e740f2b8ede788a3d1cdd5
出典メモuspto-grants-2013_07