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Methanol → 6-Benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-ol

HRID 1452471
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반응식

HRID 1452471 반응식
[C:1]1([S:7]([C:10]2[CH:11]=[C:12]3[C:17](=[CH:18][CH:19]=2)[C:16](=[O:20])[CH2:15][CH2:14][CH2:13]3)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Na].CO>O>[C:1]1([S:7]([C:10]2[CH:11]=[C:12]3[C:17](=[CH:18][CH:19]=2)[CH:16]([OH:20])[CH2:15][CH2:14][CH2:13]3)(=[O:9])=[O:8])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 5360545SodiumHCID 590217396-benzenesulfonyl-3,4-dihydro-2H-naphthalen-1-one

생성물 1

HCID 575267796-Benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-ol수율 347.8%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

6-Benzenesulfonyl-3,4-dihydro-2H-naphthalen-1-one (1.31 g, 4.6 mmol) and sodium borohidride (0.35 g, 9.3 mmol) were added to 50 mL methanol, and the reaction mixture was stirred at room temperature for one hour. Water (200 mL was then added to the reaction mixture, resulting in precipitation of white crystalls, which were collected by filtration and dried under N2 to give 1.2 g (4. 16 mmol, 90%) of 6-benzenesulfonyl- 1,2,3,4-tetrahydro-naphthalen- 1-ol, MS: 289 (M+H)+.

후처리

  1. customresulting in precipitation of white crystalls, which
  2. filtrationwere collected by filtration
  3. customdried under N2

출처 및 근거

ORD 기록
ord-97d911fc33984cbb8bdde055b19074ed
출처 데이터셋
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07473690B2

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