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

Hydrochloric Acid → (1R,2S)-2-amino-1-phenylpentan-1-ol hydrochloride

HRID 1098864
노트
인쇄 미리보기

반응식

HRID 1098864 반응식
[OH:1][C@H:2]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C@@H:3]([NH:7]C(=O)OC(C)(C)C)[CH2:4][CH2:5][CH3:6].O.[ClH:22]>C(OCC)(=O)C>[ClH:22].[NH2:7][C@@H:3]([CH2:4][CH2:5][CH3:6])[C@@H:2]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[OH:1]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 962WaterHCID 86623009tert-butyl (1R,2S)-1-hydroxy-1-phenylpentan-2-ylcarbamate

생성물 1

HCID 12843463(1R,2S)-2-amino-1-phenylpentan-1-ol hydrochloride

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매2회

반응 조건

온도
50 °C

실험 절차

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

The pure tert-butyl (1R,2S)-1-hydroxy-1-phenylpentan-2-ylcarbamate was dissolved in ethyl acetate (1.2 ml). Water (50 μl) and hydrochloric acid in ethyl acetate (1.0 ml, 1.5 M) were added. The solution was stirred at 50° C. for 90 min. A precipitation was formed. The volume was reduced to ⅔ by heavy stirring and a stream of argon gas. The stirring was continued for 1 h at r.t. The suspension was filtered and the solid was dried at 50° C. under reduced pressure for 2 h.

후처리

  1. customA precipitation
  2. customwas formed
  3. stirringby heavy stirring
  4. waitThe stirring was continued for 1 h at r.t
  5. filtrationThe suspension was filtered
  6. customthe solid was dried at 50° C. under reduced pressure for 2 h.

출처 및 근거

ORD 기록
ord-5e4f085f8098446d8496fabb1b4da597
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08143290B2

반응 노트

불러오는 중…