関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Methylimidazole | HCID 1390 | — |
| 反応物 | Tributylamine | HCID 7622 | — |
| 反応物 | Palmitoyl chloride | HCID 8206 | — |
| 反応物 | Glycine, N-formyl-, ethyl ester | HCID 76615 | — |
| 触媒 | Titanium Tetrachloride | HCID 24193 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Ethyl 2-formylamino-3-oxooctadecanoate | HCID 86638485 | 85% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08207370B2 |
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| 出典データセット | uspto-grants-2012_06 |
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| ORD ID | ord-22ebc7aedb274d4f9cc2fa0e3557ceb0 |
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| 出典メモ | uspto-grants-2012_06 |
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