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

Sodium borohydride → 5,6-Dichloro-2,3-dihydro-1H-inden-1-OL

HRID 1648208
노트
인쇄 미리보기

반응식

HRID 1648208 반응식
[BH4-].[Na+].[Cl:3][C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][C:12]=1[Cl:13])[C:9](=[O:14])[CH2:8][CH2:7]2>CO>[Cl:3][C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][C:12]=1[Cl:13])[CH:9]([OH:14])[CH2:8][CH2:7]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 229036095,6-Dichloro-2,3-dihydro-1H-inden-1-one

생성물 1

HCID 199195245,6-Dichloro-2,3-dihydro-1H-inden-1-OL

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

4.85 g of sodium borohydride were added at 0° C. to a solution of 4 g of the product of Step A in 285 ml of methanol and after stirring for one hour, the methanol was evaporated. The residue was diluted with water and excess hydride was eliminated by addition of hydrochloric acid. The mixture was extracted with ethyl acetate and the organic phase was evaporated to dryness under reduced pressure to obtain the desired product melting at 84° C.

후처리

  1. customthe methanol was evaporated
  2. additionThe residue was diluted with water and excess hydride
  3. additionwas eliminated by addition of hydrochloric acid
  4. extractionThe mixture was extracted with ethyl acetate
  5. customthe organic phase was evaporated to dryness under reduced pressure

출처 및 근거

ORD 기록
ord-e751a6ba12794190a2fe77716432c82e
출처 데이터셋
uspto-grants-1995_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05436244

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트