Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647567Generated: October 31, 2026

Triethylamine → N-[3-(Bromomethyl)phenyl]-4-(tetradecyloxy)-benzeneacetamide

https://huagongshe.com/reaction/1647567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantLithium BromideHCID 82050—
ReactantHCID 86745364HCID 86745364—
SolventTetrahydrofuranHCID 8028—
ProductN-[3-(Bromomethyl)phenyl]-4-(tetradecyloxy)-benzeneacetamideHCID 10052253—

Reaction Steps

To a stirred solution of 4.0 g of N-[3-hydroxymethyl)phenyl]-4-(tetradecyloxy)-benzeneacetamide in 100 ml of tetrahydrofuran is added 1.19 g of triethylamine followed by 1.34 g of methanesulfonyl chloride. Also added is 7.66 g of lithium bromide and continued stirring for 24 hours. The solvent is removed under vacuum and the residue is partitioned between chloroform and water followed by an additional wash of the organic layer with saturated sodium bicarbonate. The organic layer is dried and filtered through a pad of silica gel. The filtrate is evaporated to a residue which is crystallized from hexane:carbon tetrachloride to give 4.1 g of the desired product as a white powder, m.p. 116°-118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05432189
Source datasetuspto-grants-1995_07
ORD IDord-c87b6b2cf24c41f693c92c81b64c5a25
Source noteuspto-grants-1995_07