戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 566760作成日:2026年10月27日

Carbon tetrabromide → 3-(2,2-Dibromoethenyl)-2,5-dimethoxytetrahydrofuran

https://huagongshe.com/reaction/566760

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon tetrabromideHCID 11205—
反応物TriphenylphosphineHCID 11776—
反応物Tetrahydro-2,5-dimethoxyfuran-3-carbaldehydeHCID 567310—
触媒ZincHCID 23994—
溶媒DichloromethaneHCID 6344—
生成物3-(2,2-Dibromoethenyl)-2,5-dimethoxytetrahydrofuranHCID 1838042455.2%

反応手順

A mixture of Zn powder (1.65 g, 25.0 mmol), triphenylphosphine (6.54 g, 25.0 mmol), and CBr4 (8.30 g, 25.0 mmol) in dry CH2Cl2 (40 mL) was stirred at ambient temperature. After 24 hours, 2,5-dimethoxy-tetrahydrofuran-3-carboxaldehyde (2.00 g, 12.5 mmol) was added and an exothermic reaction ensued. After 30 minutes, pet ether (100 mL) was added and the resultant upper layer separated. The lower layer was twice diluted with CH2Cl2 (50 mL) and pet ether (50 mL), and the upper layer reserved. The combined upper layers were combined, passed through a pad of SiO2, and concentrated under reduced pressure at 30° C. or below to give 2.18 g (55%) of 3-(2,2-dibromoethenyl)-2,5-dimethoxy-tetrahydrofuran as a volatile colorless oil, which was a mixture of diastreomers by 1H NMR and used immediately without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06174915B1
出典データセットuspto-grants-2001_01
ORD IDord-65b77aeff52448749d4181f57527243c
出典メモuspto-grants-2001_01