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Sodium Hydroxide → 3,5-Dibromothiophenol

HRID 723625
ノート
印刷プレビュー

反応式

HRID 723625 の反応式
[OH-].[Na+].C(N(CC)C(=O)[S:7][C:8]1[CH:13]=[C:12]([Br:14])[CH:11]=[C:10]([Br:15])[CH:9]=1)C>CO>[Br:14][C:12]1[CH:13]=[C:8]([SH:7])[CH:9]=[C:10]([Br:15])[CH:11]=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

4

反応物 2

HCID 14798Sodium HydroxideHCID 20735477HCID 20735477、化合物

生成物 1

HCID 218770573,5-Dibromothiophenol収率 76.5%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
20 °C

実験手順

Sodium hydroxide (1.96 g, 49 mmol) was added to a solution of S-(3,5-dibromophenyl) diethylthiocarbamate (12 g, 32.7 mmol) (Preparation 47) in methanol (33 ml) and the mixture was heated at reflux for 15 hours. The mixture was cooled to 20° C. and concentrated under reduced pressure. The residue was partitioned between dichloromethane (90 ml) and water (250 ml) and the aqueous layer was further extracted with dichloromethane (90 ml). The combined organic layers were washed with a solution of sodium hydroxide (1N, 100 ml). The combined aqueous layers were cooled to 0° C. and the pH was adjusted to 2 by the addition of concentrated hydrochloric acid, giving a white suspension. This suspension was extracted with dichloromethane (2×250 ml) and the combined extracts were washed with brine (25 ml), dried over magnesium sulphate, filtered and concentrated under reduced pressure to leave the title compound as a yellow solid (6.7 g).

後処理

  1. temperaturethe mixture was heated
  2. temperatureat reflux for 15 hours
  3. concentrationconcentrated under reduced pressure
  4. customThe residue was partitioned between dichloromethane (90 ml) and water (250 ml)
  5. extractionthe aqueous layer was further extracted with dichloromethane (90 ml)
  6. washThe combined organic layers were washed with a solution of sodium hydroxide (1N, 100 ml)
  7. temperatureThe combined aqueous layers were cooled to 0° C.
  8. additionthe pH was adjusted to 2 by the addition of concentrated hydrochloric acid
  9. customgiving a white suspension
  10. extractionThis suspension was extracted with dichloromethane (2×250 ml)
  11. washthe combined extracts were washed with brine (25 ml)
  12. dry with materialdried over magnesium sulphate
  13. filtrationfiltered
  14. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-1bfc52ec980e4bc991444d5ac2c59569
出典データセット
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07141585B2

反応ノート

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