Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713709Generated: October 31, 2026

Dimethylformamide → HCID 68676478, compound

https://huagongshe.com/reaction/1713709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiethylamineHCID 8021—
Reactant2-(prop-2-ynyloxy)propanoic acidHCID 14743312—
ReactantHCID 67526223HCID 67526223—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
ProductHCID 68676478HCID 68676478—

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 600 mg (1.52 mM) of N-(4-chloro-2-iodophenyl)benzenesulfonamide (Preparation 120) and 0.5 ml of dimethylformamide is prepared in a microwave reaction tube and 14 mg (0.076 mM) of cuprous iodide, 27 mg (0.038 mM) of bis(triphenylphosphine)dichloropalladium, 357 mg (2.3 mM) of the ethyl ester of 2-(2-propynyloxy)propanoic acid and, finally, 0.5 ml of diethylamine are added. The mixture is heated by microwaves at 130° C. for 15 min and then cooled and hydrolyzed with 10 ml of water. The mixture is extracted three times with 15 ml of ethyl acetate and the combined organic phases are washed with water and then dried over magnesium sulfate and concentrated under reduced pressure. The residue is purified by chromatography on silica gel using a cyclohexane/ethyl acetate mixture (95/5; v/v) as the eluent to give 0.44 g of the expected compound in the form of a yellow oil (yield=69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795297B2
Source datasetuspto-grants-2010_09
ORD IDord-cb6057b1eeea46cdae30b3e85c3c3a82
Source noteuspto-grants-2010_09