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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087848Generated: October 27, 2026

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

https://huagongshe.com/reaction/1087848

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 numberUS04960798
Source datasetuspto-grants-1990_10
ORD IDord-7859d13b0a9a4139b7e32a23c9bfb489
Source noteuspto-grants-1990_10