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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646220Generated: October 27, 2026

Benzyl Bromide → 1-(Benzyloxy)-3-ethynylbenzene

https://huagongshe.com/reaction/646220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactantm-EthynylphenolHCID 139144—
Product1-(Benzyloxy)-3-ethynylbenzeneHCID 19422228609%

Reaction Steps

A mixture of 3-hydroxy-1-ethynylbenzene (4.36 g, 37 mmol), benzylbromide (6.95 g, 4.1 mmol) and K2CO3 (10.2 g, 7.4 mmol) in acetanitrile (50 ml) is stirred at room temperature for 24 hr. The insoluble material is removed by filtration and filtrate is concentrated. The crude material is purified by flash chromatography (silica gel, hexane/EtOAc:95/5) to afford the title compound as a clear oil 5.2 g (68%). 1HNMR (400 MHz, CDCl3): δ (ppm) 3.05 (s, 1H), 5.05 (s, 2H), 6.98 (d, 1H) 7.00-7.50 (m, 8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705030B2
Source datasetuspto-grants-2010_04
ORD IDord-fbd6274430d94483831aa7e4e24cbe05
Source noteuspto-grants-2010_04