Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
L-Homoserine → (2S)-2-(((9H-fluoren-9-ylmethoxy)carbonyl)amino)-4-hydroxybutanoic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | L-Homoserine | HCID 12647 | — |
| 반응물 | N-(9-Fluorenylmethoxycarbonyloxy)succinimide | HCID 134122 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Diethylether water | HCID 21584184 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | (2S)-2-(((9H-fluoren-9-ylmethoxy)carbonyl)amino)-4-hydroxybutanoic acid | HCID 15449971 | 88% |
반응 단계
L-homoserine (15 g, MW119.12, 0.126 mol) and NaHCO3 (22 g, MW84, 0.26 mol) were dissolved in water (600 mL). The solution was chilled in an ice bath, followed by addition of Fmoc-OSu (42.5 g, MW337.3, 0.126 mol) in acetone (400 mL). The mixture was stirred overnight. A mixture of ether/water (200 mL/200 mL) was added, and the solid was filtered off. The filtrate was separated and the aqueous phase was washed with ethyl twice (100 mL×2), followed by acidifying with 3N HClaq (about 100 mL) to pH3-4. The suspension was extracted with ether (200 mL×2). The combined organic phases were washed with brine once (100 mL) and dried over Na2SO4. After evaporation, white solid was obtained (weight: 38 g, yield: 88%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09446157B2 |
| 출처 데이터셋 | uspto-grants-2016_09 |
| ORD ID | ord-13d45cf8286f4c1b922e0a1388f241ba |
| 출처 메모 | uspto-grants-2016_09 |