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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463924Generated: November 2, 2026

2-Bromophenol → 1-(Benzyloxy)-2-bromobenzene

https://huagongshe.com/reaction/1463924

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromophenolHCID 7244—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
SolventAcetonitrileHCID 6342—
Product1-(Benzyloxy)-2-bromobenzeneHCID 56182897.3%

Reaction Steps

2-Bromophenol (6.7 ml, 57.8 mmole) was dissolved in 200 ml acetonitrile in a 500 ml one neck round bottom flask under nitrogen. The solution was treated successively potassium carbonate (32 g, 231 mmole) and benzyl bromide (6.9 ml, 57.8 mmole). The reaction mixture was stirred for 6 hours at room temperature. The insoluble salts were removed by filtration and the filtrate was concentrated in vacuo to a pale oil. The oil was taken up in 100 ml diethyl ether and the mixture was washed successively with 2×25 ml 1N sodium hydroxide and 1×25 ml saturated sodium chloride. The organics were dried over magnesium sulfate and were concentrated in vacuo to give 14.8 g (97%) of 2-benzyloxy-bromobenzene as a pale oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05302613
Source datasetuspto-grants-1994_04
ORD IDord-5276f0de880d4e049ee81763b26c9f62
Source noteuspto-grants-1994_04