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

HRID 1070768
ノート
印刷プレビュー

反応式

HRID 1070768 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
-10 °C

実験手順

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%).

後処理

  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.

出典と根拠

ORDレコード
ord-fbb0fcc1a2a4403ea336f5b67dca685a
出典データセット
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06903118B1

反応ノート

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