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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105895Generated: October 26, 2026

Chloroform → 4-[N-carbobenzyloxy-15-(trifluoromethyl)pentadecylamino]benzoyl chloride

https://huagongshe.com/reaction/1105895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantSodium CarbonateHCID 10340—
ReactantBenzyl chloroformateHCID 10387—
Reactant4-[15-(Trifluoromethyl)pentadecylamino]benzoic acidHCID 12831610—
SolventWaterHCID 962—
Product4-[N-carbobenzyloxy-15-(trifluoromethyl)pentadecylamino]benzoyl chlorideHCID 12831611—

Reaction Conditions

Temperature40 °C

Reaction Steps

To 15 g. 4-[15-(trifluoromethyl)pentadecylamino]benzoic acid in 200 ml. warm chloroform is added a solution of 15 g. of 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, ultimately to yield 4-[N-carbobenzyloxy-15-(trifluoromethyl)pentadecylamino]benzoyl chloride as a viscous, orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04310545
Source datasetuspto-grants-1982_01
ORD IDord-5aecfa93a1294bfa904246ef187fdedc
Source noteuspto-grants-1982_01