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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721740Generated: October 31, 2026

Ethanol → Ethyl 4-trichloroacetamido-5-hexenoate

https://huagongshe.com/reaction/1721740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTrichloroacetonitrileHCID 11011—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 6-hydroxy-4-hexenoateHCID 53641333—
SolventDiethyl EtherHCID 3283—
ProductEthyl 4-trichloroacetamido-5-hexenoateHCID 11055787727.1%

Reaction Steps

Sodium hydride (0.03 g of a 50% dispersion in oil, 0.5 mmol, was added to a solution of ethyl 6-hydroxy-4-hexenoate (0.7 g, 5 mmol) and trichloroacetonitrile (0.6 g, 5 mmol) in anhydrous ether (50 mL) under N2 at 0° C. After 1 H, ethanol (0.5 mmol) was added and the solvent was removed in vacuo. The formation of the imidate was controled by NMR (NH,~8.5 ppm). A solution of the crude imidate in xylene (30 mL) was heated at reflux 48 H. Then the solvent was removed in vacuo and the residue was purified by flash chromatography on SiO2. (eluant AcOEt: hexane, 2:8) to give the title product (1.1 g, ~70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05512698
Source datasetuspto-grants-1996_04
ORD IDord-d680ef5728934538954b638cdecc0195
Source noteuspto-grants-1996_04