홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Aluminium lithium hydride → (2S,3S)-2-amino-3-ethyl-5,5,5-trifluoropentan-1-ol

HRID 1594296
노트
인쇄 미리보기

반응식

HRID 1594296 반응식
[N:1]([C@@H:4]([C@@H:8]([CH2:14][CH3:15])[CH2:9][C:10]([F:13])([F:12])[F:11])[C:5](O)=[O:6])=[N+]=[N-].[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[NH2:1][C@@H:4]([C@@H:8]([CH2:14][CH3:15])[CH2:9][C:10]([F:11])([F:12])[F:13])[CH2:5][OH:6]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21226445Aluminium lithium hydrideHCID 86594493HCID 86594493, 화합물

생성물 1

HCID 86594491(2S,3S)-2-amino-3-ethyl-5,5,5-trifluoropentan-1-ol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
40 °C

실험 절차

(2S,3S)-2-Azido-3-ethyl-5,5,5-trifluoro-pentanoic acid was dissolved in THF (5 mL) at 0° C. and lithium aluminum hydride (1 M solution in THF) (mL, 1 mmol) was added. The resulting solution was stirred at 40° C. for 2 h. The reaction was quenched by sequential addition of water (60 μL), 15% aqueous sodium hydroxide (60 μL), and water (150 μL) with vigorous stirring between each addition. The mixture was then filtered and concentrated to give (2S, 3S)-2-amino-3-ethyl-5,5,5-trifluoro-pentan-1-ol.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. customThe reaction was quenched by sequential addition of water (60 μL), 15% aqueous sodium hydroxide (60 μL), and water (150 μL)
  2. stirringwith vigorous stirring between each addition
  3. filtrationThe mixture was then filtered
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-98140cb6ade2401d8fbfcd7d69b61582
출처 데이터셋
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07300951B2

반응 노트

불러오는 중…