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

Sodium → (S)-1-(4-chloro-3-fluorophenyl)propane-1,3-diol

HRID 1774159
노트
인쇄 미리보기

반응식

HRID 1774159 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]2[O:10][C@@H:9]2[CH2:11][OH:12])=[CH:4][C:3]=1[F:13].[Na].[H-].[Al+3].[H-].[H-]>COCCOC.CCOCC>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@@H:8]([OH:10])[CH2:9][CH2:11][OH:12])=[CH:4][C:3]=1[F:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 5360545SodiumHCID 21584524AluminiumhydrideHCID 86696658((2R,3R)-3-(4-chloro-3-fluorophenyl)oxiran-2-yl)methanol

생성물 1

HCID 86696659(S)-1-(4-chloro-3-fluorophenyl)propane-1,3-diol수율 98.55%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 8071
1,2-Dimethoxyethane
용매

반응 조건

온도
0 °C

실험 절차

((2R,3R)-3-(4-Chloro-3-fluorophenyl)oxiran-2-yl)methanol (10.55 g, 52.07 mmol) was dissolved in 1,2-dimethoxyethane (150 mL) and cooled to 0° C. Sodium bis (2-methohyethoxy) aluminum hydride (“Red-Al”) (17.46 mL, 57.28 mmol) was added dropwise. The mixture was agitated for 3 hours at room temperature, diluted with ether (250 mL) and quenched with HCl solution (20 mL, 6M HCl+60 mL water). After agitating for 30 minutes, the aqueous phase was separated and extracted twice with ethyl acetate. The combined organics were washed with brine, dried with MgSO4, and evaporated to give (S)-1-(4-chloro-3-fluorophenyl)propane-1,3-diol (10.5 g, 51.31 mmol, 98.55% yield) as thick oil.

후처리

  1. customquenched with HCl solution (20 mL, 6M HCl+60 mL water)
  2. stirringAfter agitating for 30 minutes
  3. customthe aqueous phase was separated
  4. extractionextracted twice with ethyl acetate
  5. washThe combined organics were washed with brine
  6. dry with materialdried with MgSO4
  7. customevaporated

출처 및 근거

ORD 기록
ord-bb596d66141a4fa2a27ee9b16fc2818f
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09259470B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트