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HRID 222827作成日:2026年10月26日

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

https://huagongshe.com/reaction/222827

反応式

関与物質

役割名称HCID仕込み量
反応物1-MethylimidazoleHCID 1390—
反応物TributylamineHCID 7622—
反応物Palmitoyl chlorideHCID 8206—
反応物Glycine, N-formyl-, ethyl esterHCID 76615—
触媒Titanium TetrachlorideHCID 24193—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 2-formylamino-3-oxooctadecanoateHCID 8663848585%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207370B2
出典データセットuspto-grants-2012_06
ORD IDord-22ebc7aedb274d4f9cc2fa0e3557ceb0
出典メモuspto-grants-2012_06