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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280874Generated: November 2, 2026

Benzyl Bromide → HCID 15895031, compound

https://huagongshe.com/reaction/1280874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant2,3-DimethylfuranHCID 34337—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15895031HCID 1589503178.2%

Reaction Steps

At −78° C., to a stirred solution of commercial 2,3-dimethylfuran (50 g, 0.520 mol) in THF (2.6 L) was add dropwise 1.6M n-BuLi/hexanes (325 mL, 0.520 mol). After the addition was complete, the dry ice/acetone bath was removed and the reaction was stirred for 1 h. At −78° C., to the reaction was added dropwise commercial benzyl bromide (62 mL, 0.520 mol). After the addition was complete the reaction was stirred at −78° C. for 6 h, the dry ice/acetone bath was removed and the reaction was stirred for 7 days. The reaction was concentrated in vacuo and purified on silica gel eluting with hexane to give 75.70 g (78%) of the title compound as a clear oil; 1H NMR (DMSO-d6) δ 1.83 (s, 3H), 2.08 (s, 3H), 3.83 (s, 2H), 5.83 (s, 1H), 7.16-7.30 (m, 5H). mass spectrum (EI), m/z 186 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451845B1
Source datasetuspto-grants-2002_09
ORD IDord-5c261543a1d34178a4e26cffaed1ae15
Source noteuspto-grants-2002_09