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

3-Nitro-6,7,8,9-tetrahydro-5H-benzo[a]cyclohepten-5-one → 3-nitro-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ol

HRID 274062
노트
인쇄 미리보기

반응식

HRID 274062 반응식
[N+:1]([C:4]1[CH:15]=[CH:14][C:7]2[CH2:8][CH2:9][CH2:10][CH2:11][C:12](=[O:13])[C:6]=2[CH:5]=1)([O-:3])=[O:2].[BH4-].[Na+]>CO>[N+:1]([C:4]1[CH:15]=[CH:14][C:7]2[CH2:8][CH2:9][CH2:10][CH2:11][CH:12]([OH:13])[C:6]=2[CH:5]=1)([O-:3])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 3444873-Nitro-6,7,8,9-tetrahydro-5H-benzo[a]cyclohepten-5-oneHCID 4311764Sodium borohydride

생성물 1

HCID 223918023-nitro-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ol수율 96.3%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a suspension of 3-nitro-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-one (7.0 g) in methanol (70 ml), sodium borohydride (1.29 g) was added portionwise at 21°-30° C. and the whole was stirred for 1 hour. The solution was poured into ice water (210 ml) and the resulting precipitate was collected by filtration, washed with water and dried to give 3-nitro-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ol (6.81 g).

후처리

  1. additionwas added portionwise at 21°-30° C.
  2. filtrationthe resulting precipitate was collected by filtration
  3. washwashed with water
  4. customdried

출처 및 근거

ORD 기록
ord-8725762c71a84aa793e45c0776afc080
출처 데이터셋
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05387710

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트