Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetrahydrofuran → N-(cholest-5-ene-3beta-oxycarbonyl)glycylglycine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Glycylglycine | HCID 11163 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | C28H45ClO2 | HCID 54236888 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | N-(cholest-5-ene-3beta-oxycarbonyl)glycylglycine | HCID 131717552 | 80.8% |
반응 단계
Sodium hydrogencarbonate (0.168 g) and tetrahydrofuran (20 ml) were added to a suspension of glycylglycine (0.15 g) in water (20 ml). After tetrahydrofuran (20 ml) and cholesteryl chloroformate (0.898 g) were added to the resulting transparent solution at 0° C., the mixture was stirred for an hour. The reaction mixture was concentrated under reduced pressure and, methanl (10 ml) and chloroform (10 ml) were added to the residue. By filtration, the transparent solution was obtained. The solvent was distilled off to give crude crystals (0.98 g). The crude crystals were then purified by silica gel chromatography to give N-(cholest-5-ene-3β-oxycarbonyl)glycylglycine (0.5 g) as white powders.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05152999 |
| 출처 데이터셋 | uspto-grants-1992_10 |
| ORD ID | ord-c01942f2ad344ee7b3deac1007c75775 |
| 출처 메모 | uspto-grants-1992_10 |