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Hydrochloric Acid → 6-Bromo-5,8-dimethylthiochroman-4-ol

HRID 964390
ノート
印刷プレビュー

反応式

HRID 964390 の反応式
[Br:1][C:2]1[C:3]([CH3:14])=[C:4]2[C:9](=[C:10]([CH3:12])[CH:11]=1)[S:8][CH2:7][CH2:6][C:5]2=[O:13].[BH4-].[Na+].Cl>CO>[Br:1][C:2]1[C:3]([CH3:14])=[C:4]2[C:9](=[C:10]([CH3:12])[CH:11]=1)[S:8][CH2:7][CH2:6][CH:5]2[OH:13]
参加物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 313Hydrochloric AcidHCID 4311764Sodium borohydrideHCID 152784955,8-Dimethyl-6-bromothiochroman-4-one

生成物 1

HCID 234507086-Bromo-5,8-dimethylthiochroman-4-ol収率 95%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

In a 100-ml eggplant type flask, 5.0 g (18.4 mmol) of 6-bromo-5,8-dimethylthiochroman-4-one as a halogenated thiochroman-4-one compound was dissolved in 30 ml of methanol, and 0.35 g (9.2 mmol, 0.5 equivalent) of sodium borohydride as a reducing agent was added at room temperature. The reaction mixture was stirred for 2 hours, then, diluted hydrochloric acid was added, and the mixture was extracted with ethyl acetate. An organic layer was washed with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate, and then solvent was distilled off to give 0.49 g (yield 95%) of 6-bromo-5,8-dimethylthiochroman-4-ol.

後処理

  1. extractionthe mixture was extracted with ethyl acetate
  2. washAn organic layer was washed with a saturated sodium chloride aqueous solution
  3. dry with materialdried over anhydrous sodium sulfate
  4. distillationsolvent was distilled off

出典と根拠

ORDレコード
ord-8e6677bfc62945339e24ee362eb0107e
出典データセット
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05767289

反応ノート

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