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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222820Generated: October 25, 2026

1-Methylimidazole → Ethyl 2-acetylamino-3-oxooctadecanoate

https://huagongshe.com/reaction/222820

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
ReactantTributylamineHCID 7622—
ReactantPalmitoyl chlorideHCID 8206—
ReactantEthyl acetamidoacetateHCID 74702—
CatalystTitanium TetrachlorideHCID 24193—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-acetylamino-3-oxooctadecanoateHCID 8663848488%

Reaction Steps

A methylene chloride solution (5.0 ml) of N-acetylglycine ethyl ester (72.5 mg, 0.50 mmol) and N-methylimidazole (50.4 mg, 0.61 mmol) was cooled to −45° C., and a methylene chloride solution (0.5 ml) of palmitoyl chloride (142.6 mg, 0.50 mmol) was added thereto in nitrogen atmosphere. After the mixture was stirred for 20 minutes at the same temperature, a methylene chloride solution (0.5 ml) of titanium tetrachloride (340.4 mg, 1.78 mmol) and a methylene chloride solution (0.5 ml) of tributylamine (372.4 mg, 2.01 mmol) were added thereto. The resulting mixture was stirred for 2 hours at −45° C. Water was added thereto, and the mixture was heated to room temperature, and the organic layer was separated. Further, the water layer was extracted twice with methylene chloride, and the organic layers were combined and dried with magnesium sulfate. After the solvent was removed in reduced pressure, the obtained crude product was purified by silica gel chromatography (Kieselgel 60 manufactured by Merck, hexane:ethyl acetate=3:2) to obtain the title compound (148.8 mg, yield: 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207370B2
Source datasetuspto-grants-2012_06
ORD IDord-ab379f77c0db4113a3553eaeaf09abcf
Source noteuspto-grants-2012_06