Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetic Acid → N-Benzyloxycarbonyl-2-amino-2-[4-propoxybenzyl]-ethanol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | N-benzyloxycarbonyl-3-[4-propoxyphenyl]-alanine-methyl ester | HCID 22940772 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | tert-Butyl methyl ether | HCID 15413 | — |
| 생성물 | N-Benzyloxycarbonyl-2-amino-2-[4-propoxybenzyl]-ethanol | HCID 67688130 | — |
반응 단계
4.15 g (11.2 mmol) of N-benzyloxycarbonyl-3-[4-propoxyphenyl]-alanine-methyl ester is dissolved in 20 ml of tert-butyl methyl ether and mixed with 0.17 g (4.5 mmol) of sodium borohydride. At 0° C., 6 ml of methanol is added and it is stirred for three hours under argon at a temperature below 5° C. Then, 0.8 ml of acetic acid, dissolved in 3 ml of tetrahydrofuran, is added, mixed with 3 ml of water and stirred for ten minutes at room temperature. The organic phase is separated, washed with water and dried on sodium sulfate. The drying agent is suctioned off, the filtrate is concentrated by evaporation and the residue is chromatographed for purification on silica gel (eluent: ethyl acetate/hexane).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05885548 |
| 출처 데이터셋 | uspto-grants-1999_03 |
| ORD ID | ord-618e053887574cc6b247533a9ccc844b |
| 출처 메모 | uspto-grants-1999_03 |