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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870972Generated: October 25, 2026

Triethylamine → 1-(2-Bromoethyl)-2-ethoxybenzene

https://huagongshe.com/reaction/1870972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantLithium BromideHCID 82050—
Reactant2-(2-Ethoxyphenyl)ethanolHCID 251271—
SolventDichloromethaneHCID 6344—
Product1-(2-Bromoethyl)-2-ethoxybenzeneHCID 18694511—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1.35 g (8.12 mmol) of 2-ethoxyphenethyl alcohol and 2.05 g (20.03 mmol) of triethylamine in 15 ml of dichloromethane was slowly added 1.86 g (16.24 mmol) of methanesulfonyl chloride at 0° C. The reaction mixture was stirred at 0° C. for 2 h and was poured into 200 ml of mixed solution of hexanelether(1:1). It was washed with 30 ml of water, dried over MgSO4, filtered through a plug of silica gel and concentrated. The residue was dissolved in 30 ml of acetone and 2.82 g (32.48 mmol) of lithium bromide was added slowly at 0° C. The reaction mixture was refluxed for 5 h and volatiles were removed. The residue was added 150 ml of ether, washed with water (30 ml ×2), dried over MgSO4, filtered through a plug of silica gel and concentrated to give 2-ethoxyphenethyl bromide as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06100293
Source datasetuspto-grants-2000_08
ORD IDord-f93043d0b6b4407da71f99426c65de65
Source noteuspto-grants-2000_08