Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731837Generated: October 25, 2026

Boron trifluoride etherate → N-(2-chlorobenzyl)-3-methoxyphenylacetamide

https://huagongshe.com/reaction/1731837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantTriethylamineHCID 8471—
Reactant(3-Methoxyphenyl)acetic acidHCID 15719—
Reactant2-ChlorobenzylamineHCID 66648—
SolventTolueneHCID 1140—
ProductN-(2-chlorobenzyl)-3-methoxyphenylacetamideHCID 2089226—

Reaction Steps

A mixture of 12.5 g of 3-methoxyphenylacetic acid, 21.2 g of 2-chlorobenzylamine, 15.1 g of triethylamine, 19.3 ml of borontrifluoride etherate, and 500 ml of toluene was stirred under reflux for 18 hours using a Dean-Stark moisture trap and allowed to cool. The mixture was extracted with aqueous sodium hydroxide, dilute hydrochloric acid, and water. The remaining organic solution was then evaporated and the residue crystallized from hexane to yield N-(2-chlorobenzyl)-3-methoxyphenylacetamide as a yellow solid, m.p. 89°-91° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04623662
Source datasetuspto-grants-1986_11
ORD IDord-e5ff32d385f54149832b99453966ef75
Source noteuspto-grants-1986_11