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HRID 70553作成日:2026年10月26日

tert-Butyl (triphenylphosphoranylidene) acetate → Tert-butyl 3-(6-bromo-2-methoxypyridin-3-yl)acrylate

https://huagongshe.com/reaction/70553

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl (triphenylphosphoranylidene) acetateHCID 256127—
反応物6-Bromo-2-methoxynicotinaldehydeHCID 12269213—
溶媒ChloroformHCID 6212—
生成物Tert-butyl 3-(6-bromo-2-methoxypyridin-3-yl)acrylateHCID 86658007100%

反応手順

(tert-Butoxycarbonylmethylene)triphenylphosphorane (1.74 g) was added to a solution of 6-bromo-2-methoxynicotinaldehyde (500 mg) in chloroform (5 mL) under ice-cooling, followed by stirring for one hour. The solvent was evaporated from the reaction solution under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1) to give tert-butyl 3-(6-bromo-2-methoxypyridin-3-yl)acrylate as a colorless oil (726 mg, 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822503B2
出典データセットuspto-grants-2014_09
ORD IDord-0d67ace4cd5b44c18847e836ae37bb44
出典メモuspto-grants-2014_09