Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → N-6-bromohexanoyl-L-leucine ethyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 6-Bromohexanoyl chloride | HCID 89848 | — |
| 반응물 | L-Leucine, ethyl ester, hydrochloride (1:1) | HCID 11658447 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Ammonium Chloride | HCID 25517 | — |
| 생성물 | N-6-bromohexanoyl-L-leucine ethyl ester | HCID 22866411 | 80% |
반응 단계
A stirred suspension of L-leucine ethyl ester hydrochloride (8.38 g, 45 mmol) in dry THF (80 ml) at room temperature was treated with triethylamine (6.3 ml, 45 mmol). The reaction mixture was treated with 6-bromohexanoyl chloride (6.91 ml, 45 mmol). The reaction mixture was stirred for 4 h at room temperature and then diluted with a mixture of saturated aqueous ammonium chloride and ethyl acetate. The organic layer was separated, washed with saturated aqueous ammonium chloride, dried over anhydrous sodium sulphate, filtered and evaporated under reduced pressure to give N-6-bromohexanoyl-L-leucine ethyl ester (12.1 g, 80%) as an oil which was used for the next step without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05563151 |
| 출처 데이터셋 | uspto-grants-1996_10 |
| ORD ID | ord-825b0c937ac6420892ded97bbd91ba54 |
| 출처 메모 | uspto-grants-1996_10 |