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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274538Generated: October 30, 2026

(3-Bromopropyl)benzene → HCID 10937342, compound

https://huagongshe.com/reaction/274538

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Bromopropyl)benzeneHCID 12503—
Reactant4-(Benzyloxy)-3-methoxybenzaldehydeHCID 75506—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
SolventPentaneHCID 8003—
ProductHCID 10937342HCID 10937342—

Reaction Steps

A solution of 20.0 g of 3-phenylpropyl bromide in 300 ml of ether is treated at -60° while stirring within 15 minutes with a solution of 71.8 ml of tert.butyllithium (1.4 molar) in pentane. After 10 minutes there is added dropwise at this temperature within 15 minutes a solution of 22.14 g of vanillin benzyl ether in 200 ml of ether, whereupon the mixture is stirred for an additional 2 hours. The mixture is poured into 11 of ice-water and extracted three times with 500 ml of ethyl acetate each time. The organic phase is washed twice with 200 ml of water each time, dried over sodium sulfate and evaporated. The oil obtained is chromatographed on 1 kg of silica gel with methylene chloride. The crystals obtained are recrystallized from ether/pentane. There is obtained 4-(benzyloxy)-3-methoxy-α-(3-phenylpropyl)benzyl alcohol in the form of colorless crystals of m.p. 71°-73°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389653
Source datasetuspto-grants-1995_02
ORD IDord-5fb2bd81f3044d8b9abd2f55ad9efbe6
Source noteuspto-grants-1995_02