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Hydrochloric Acid → 3,4-Difluorobenzyl Mercaptan

HRID 1455011
ノート
印刷プレビュー

反応式

HRID 1455011 の反応式
N[C:2](N)=[S:3].[F:5][C:6]1[CH:7]=[C:8]([CH:11]=[CH:12][C:13]=1[F:14])CBr.Cl>C(O)C.[OH-].[Na+]>[F:5][C:6]1[CH:7]=[C:8]([CH2:2][SH:3])[CH:11]=[CH:12][C:13]=1[F:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 313Hydrochloric AcidHCID 5814364-(Bromomethyl)-1,2-difluorobenzeneHCID 2723790Thiourea

生成物 1

HCID 27614283,4-Difluorobenzyl Mercaptan

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 14798Sodium Hydroxide溶媒

実験手順

Thiourea (5.0 g) was added to a solution of 3,4-difluorobenzyl bromide (13.6 g) in ethanol (100 ml). The mixture was heated at reflux for 3 h before removal of the volatiles in vacuo. The crude solid was suspended in aqueous sodium hydroxide solution (1.6M, 110 ml) and heated at reflux for 3 h before allowing to cool to room temperature. The reaction was acidified with concentrated hydrochloric acid and the organics extracted with ether (200 ml). The organic layer was washed with saturated sodium bicarbonate solution (2×50 ml), brine (20 ml), dried (MgSO4), and concentrated in vacuo to provide the subtitle product as a colourless oil. Yield 11.1 g

後処理

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 3 h before removal of the volatiles in vacuo
  3. temperatureheated
  4. temperatureat reflux for 3 h
  5. extractionthe organics extracted with ether (200 ml)
  6. washThe organic layer was washed with saturated sodium bicarbonate solution (2×50 ml), brine (20 ml)
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-09df2e4c3698490e81152dac35327843
出典データセット
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07482355B2

反応ノート

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