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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4282Generated: October 26, 2026

Dimethylamine → 2-(2-Iodo-5-methoxyphenyl)-N,N-dimethylacetamide

https://huagongshe.com/reaction/4282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantDichloromethaneHCID 6344—
ReactantOxalyl chlorideHCID 65578—
Reactant2-(2-Iodo-5-methoxyphenyl)acetic acidHCID 820071—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Product2-(2-Iodo-5-methoxyphenyl)-N,N-dimethylacetamideHCID 14025497—

Reaction Steps

A 16.7 g (0.19 mole) sample of oxalyl chloride was added dropwise at 0° C. to a solution of 50.0 g (0.17 mole) of 2-iodo-5-methoxybenzeneacetic acid in 310 ml dry toluene and 31.7 ml of DMF. The mixture was allowed to warm to room temperature and stir for 16 hours. The solution was cooled to 0° C. and dimethylamine gas was admitted until the mixture was strongly basic. The mixture was allowed to warm to room temperature and stir for three hours and methylene chloride was added. The organic layer was washed with water, dilute hydrochloric acid, and sodium hydroxide. The organic layer was dried with MgSO4 and evaporated in vacuo to give 54.2 g of N,N-dimethyl-2-iodo-5-methoxybenzeneacetamide, mp 86°-89° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04725602
Source datasetuspto-grants-1988_02
ORD IDord-376b3b80298747838d4894a89b3c46a4
Source noteuspto-grants-1988_02