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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671747Generated: October 25, 2026

Chloroform → N-lauroyl-L-valine cyclohexylamide

https://huagongshe.com/reaction/1671747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantCyclohexylamineHCID 7965—
ReactantN-(1-Oxododecyl)-L-valineHCID 26658—
ReactantN-Hydroxysuccinimide hydrateHCID 18987794—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductN-lauroyl-L-valine cyclohexylamideHCID 1152376444%

Reaction Steps

61 mg (0.20 mmol) of N-lauroyl-L-valine and 39 mg (0.26 mmol) of N-hydroxysuccinimide monohydrate were dissolved into 3.0 mL of dried chloroform. 50 mg (0.26 mmol) of 1-ethyl-3-(3-dimethylpropyl)carbodiimide hydrochloride was added thereto under argon atmosphere and in the ice bath, and stirred at 0° C. for 3 hours. 35 μL of triethylamine and 35 μL of cyclohexylamine were added thereto and stirred at room temperature overnight. Then, 20 mL of ethyl acetate was added thereto and washed with 25 mL of 0.2N hydrochloric acid, 20 mL of water and 20 mL of a saturated aqueous solution of sodium hydrogen carbonate. The mixture was then dried with anhydrous sodium sulfate and condensed under reduced pressure. The residue was purified with a thin-layer chromatography (silica gel, chloroform:methanol=20:1) to obtain 34 mg of N-lauroyl-L-valine cyclohexylamide (0.089 mmol, yield 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994353B2
Source datasetuspto-grants-2011_08
ORD IDord-9354f11cead54404a1a6b46abc7bb267
Source noteuspto-grants-2011_08