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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566760Generated: October 25, 2026

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

https://huagongshe.com/reaction/566760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantTetrahydro-2,5-dimethoxyfuran-3-carbaldehydeHCID 567310—
CatalystZincHCID 23994—
SolventDichloromethaneHCID 6344—
Product3-(2,2-Dibromoethenyl)-2,5-dimethoxytetrahydrofuranHCID 1838042455.2%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174915B1
Source datasetuspto-grants-2001_01
ORD IDord-65b77aeff52448749d4181f57527243c
Source noteuspto-grants-2001_01