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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8409Generated: October 25, 2026

Benzyl Chloride → 1,4-Bis(benzyloxy)-2-butene

https://huagongshe.com/reaction/8409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
Reactant2-Butene-1,4-diolHCID 8065—
ReactantSodium HydroxideHCID 14798—
CatalystTetrabutylammonium BromideHCID 74236—
Product1,4-Bis(benzyloxy)-2-buteneHCID 4054109114.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

To 48% aqueous sodium hydroxide (127.8 g) was added tetra-n-butylammonium bromide (3.3 g, 10 mmol). The mixture was heated to 60° C. To the mixture was added 2-butene-1,4-diol (17) (30.0 g, 340 mmol), to which was added dropwise benzyl chloride (94.8 g, 743 mmol) at 80±15° C. The mixture was stirred at the same temperature for 2 hours. The reaction mixture was cooled down, and separated after the addition of water (90 ml). To the organic layer was added sulfuric acidic brine. The solution was neutralized by aqueous sodium hydrogen carbonate, separated, mixed with ethyl acetate and concentrated under reduced pressure to yield the objective (18) (104.5 g, quantitative) as an oil residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087764B2
Source datasetuspto-grants-2006_08
ORD IDord-4caad36be5ac4269aa3917d91c05067e
Source noteuspto-grants-2006_08