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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278302Generated: November 1, 2026

Chloroform → 4-(N-carbobenzyloxy-allylamino)phenylacetyl chloride

https://huagongshe.com/reaction/1278302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantSodium CarbonateHCID 10340—
ReactantBenzyl chloroformateHCID 10387—
ReactantAcetic acid, 2-(p-(allylamino)phenyl)-HCID 38316—
SolventWaterHCID 962—
Product4-(N-carbobenzyloxy-allylamino)phenylacetyl chlorideHCID 54085438—

Reaction Conditions

Temperature40 °C

Reaction Steps

To 15 g. 4-(allylamino)phenylacetic acid in 200 ml. warm chloroform is added a solution of 12 g. sodium carbonate in 150 ml. water. To the vigorously stirred solution is added 10 g. carbobenzyloxy chloride. After 2 hours stirring at 40° C., the layers are separated, washed three times with 1N hydrochloric acid, dried, and evaorated to an oil. The oil is dissolved in 300 ml. toluene, treated with 15 ml. thionyl chloride and the solution is refluxed for 5 hours. The solvents are evaporated and the residue is dissolved three times in toluene, evaporating each time ultimately to yield 4-(N-carbobenzyloxy-allylamino)phenylacetyl chloride as a viscous, orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04281019
Source datasetuspto-grants-1981_07
ORD IDord-4801e610fd864cbc99ef41ee1f028d61
Source noteuspto-grants-1981_07