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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 222827생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/222827

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylimidazoleHCID 1390—
반응물TributylamineHCID 7622—
반응물Palmitoyl chlorideHCID 8206—
반응물Glycine, N-formyl-, ethyl esterHCID 76615—
촉매Titanium TetrachlorideHCID 24193—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물Ethyl 2-formylamino-3-oxooctadecanoateHCID 8663848585%

반응 단계

A methylene chloride solution (100 ml) of N-formylglycine ethyl ester (1.31 g, 10 mmol) and N-methylimidazole (985.4 mg, 12 mmol) was cooled to −45° C., and a methylene chloride solution (10 ml) of palmitoyl chloride (2.85 mg, 10 mmol) was added thereto in nitrogen atmosphere. After the mixture was stirred for 20 minutes at the same temperature, a methylene chloride solution (10 ml) of titanium tetrachloride (6.78 mg, 35 mmol) and a methylene chloride solution (10 ml) of tributylamine (7.42 g, 40 mmol) were added thereto. The resulting mixture was stirred for 3 hours at −45° C. After 100 ml of 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. 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, solely ethyl acetate) to obtain the title compound (3.15 mg, yield: 85%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207370B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-22ebc7aedb274d4f9cc2fa0e3557ceb0
출처 메모uspto-grants-2012_06