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

Water → (2S)-3-Phenylpropane-1,2-diol

HRID 223788
노트
인쇄 미리보기

반응식

HRID 223788 반응식
[H-].[H-].[H-].[H-].[Li+].[Al+3].[C:7]1([C@:13](C)(O)[C:14]([OH:16])=O)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.O.[OH-].[Na+].[O:22]1CCC[CH2:23]1>>[OH:22][CH2:23][C@@H:14]([OH:16])[CH2:13][C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 5

HCID 962WaterHCID 8028Tetrahydrofuran2회HCID 14798Sodium HydroxideHCID 445144(S)-Atrolactic acidHCID 21226445Aluminium lithium hydride

생성물 1

HCID 446127(2S)-3-Phenylpropane-1,2-diol

실험 절차

There were dropped into a suspension of 50 grams of LiAlH4 in 750 ml of tetrahydrofuran (THF) cooled to 0° C. within 3 hours 83.1 grams of (S)-phenyl lactic acid dissolved in 250 ml of THF. The reaction mixture was boiled for 2 hours under reflux, after cooling treated portionwise with water and 43 ml of 4 N-NaOH and boiled for 0.5 hour under reflux. The white precipitate was filtered off and carefully washed with hot THF. The solvent was distilled off from the combined filtrates and the crude product fractionally distilled. There were obtained 64.6 grams of (S)-1,2-dihydroxy-3-phenyl-propane of boiling point 101°-102° C. (0.001 mbar).

후처리

  1. temperatureunder reflux
  2. temperatureafter cooling
  3. waitboiled for 0.5 hour
  4. temperatureunder reflux
  5. filtrationThe white precipitate was filtered off
  6. washcarefully washed with hot THF
  7. distillationThe solvent was distilled off from the combined filtrates
  8. distillationthe crude product fractionally distilled

출처 및 근거

ORD 기록
ord-563f43a0cf5b4d88ab3500786c92f5d4
출처 데이터셋
uspto-grants-1982_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04356324

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트