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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903409Generated: October 25, 2026

Chloroform → N-carbobenzyloxy-4-(8-cyclohexyloctylamino)benzoyl chloride

https://huagongshe.com/reaction/903409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantSodium CarbonateHCID 10340—
ReactantBenzyl chloroformateHCID 10387—
Reactant4-(8-Cyclohexyloctylamino)benzoic acidHCID 20475772—
SolventWaterHCID 962—
ProductN-carbobenzyloxy-4-(8-cyclohexyloctylamino)benzoyl chlorideHCID 20475782—

Reaction Conditions

Temperature40 °C

Reaction Steps

To 15 g. 4-(8-cyclohexyloctylamino)benzoic acid in 200 ml. warm chloroform is added 15 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 1 N hydrochloric acid, dried, and evaporated 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 to yield a viscous, orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04227014
Source datasetuspto-grants-1980_10
ORD IDord-d6d3637114584028b6941b0aef82f943
Source noteuspto-grants-1980_10