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HRID 1069205作成日:2026年10月26日

Benzaldehyde → 2,3-Dimethyl-5-(alpha-hydroxybenzyl)thiophene

https://huagongshe.com/reaction/1069205

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物Ammonium ChlorideHCID 25517—
反応物2,3-DimethylthiopheneHCID 34295—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物2,3-Dimethyl-5-(alpha-hydroxybenzyl)thiopheneHCID 1163712680%

反応条件

温度0 °C

反応手順

n-Butyl lithium (19.6 ml, 49.1 mmol, 2.5 N in hexanes) was added dropwise to a stirred solution of 2,3-dimethyl-thiophene (5.0 g, 44.6 mmol) in THF (100 mL) at −78° C. under a dry nitrogen atmosphere. The solution was warmed to 0° C. for 30 min and recooled to −78° C. whereupon benzaldehyde (5.0 mL, 49.1 mmol ) was added. After an additional 45 minutes, sat. aq. ammonium chloride was added and the reaction mixture was partitioned between water and ether. The ether phase was washed with brine and concentrated. The resultant oil was triturated with pet. ether to provide the title compound as a white solid (7.77 g, 80%): mp 80-81° C.: NMR (CDCl3); δ7.45 (ddd, J=8, 1, 1 Hz, 2H), 7.37 (ddd, J=8, 8, 1 Hz, 2H), 7.3 (m, 1H), 6.57 (s, 1H), 6.93 (s, 1H, OH), 2.29 (s, 3H), 2.05 (s, 3H); MS (EI) (M+) 218 (45%, MI): Anal. Calc. for C13H14OS: C, 71.52; H, 6.46; N, 0.00. Found: C, 71.41; H, 6.42; N, 0.09.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06251936B1
出典データセットuspto-grants-2001_06
ORD IDord-e268daf6277a433eaa5545f6f72e4a0e
出典メモuspto-grants-2001_06