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Water → 6,11-Dihydrodibenzo[b,e]thiepin-11-ol

HRID 1070768
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인쇄 미리보기

반응식

HRID 1070768 반응식
[CH2:1]1[C:11]2[C:10](=[O:12])[C:9]3[CH:13]=[CH:14][CH:15]=[CH:16][C:8]=3[CH2:7][S:6][C:5]=2[CH:4]=[CH:3][CH2:2]1.[BH4-].[Na+].O>CO>[CH:1]1[C:11]2[CH:10]([OH:12])[C:9]3[CH:13]=[CH:14][CH:15]=[CH:16][C:8]=3[CH2:7][S:6][C:5]=2[CH:4]=[CH:3][CH:2]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 4311764Sodium borohydrideHCID 223976646.1-Dihydro-dibenzo[b,e]thiepin-11-one

생성물 1

HCID 6014316,11-Dihydrodibenzo[b,e]thiepin-11-ol

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
-10 °C

실험 절차

48 g (212 mmol) 6.1-dihydro-dibenzo[b,e]thiepin-11-one are dissolved in 480 ml absolute methanol and cooled to ca. −10° C. 19.2 g (507 mmol) sodium borohydride is added portion wise to this solution. The mixture is stirred for three hours at RT without further cooling. After the careful addition of 30 ml water, the suspension is concentrated under vacuum. The residue is taken up in 500 ml dichloromethane and washed twice each with 150 ml water. The organic phase is dried over sodium sulfate and the solvent is removed under vacuum. The residue is crystallized from 180 ml toluene. Colorless crystals of MP. 108° C.: Yield 41.2 g (85%).

후처리

  1. concentrationthe suspension is concentrated under vacuum
  2. washwashed twice each with 150 ml water
  3. dry with materialThe organic phase is dried over sodium sulfate
  4. customthe solvent is removed under vacuum
  5. customThe residue is crystallized from 180 ml toluene
  6. customColorless crystals of MP. 108° C.

출처 및 근거

ORD 기록
ord-fbb0fcc1a2a4403ea336f5b67dca685a
출처 데이터셋
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06903118B1

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