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Hydrochloric Acid → (R)-1-(4-Chloro-3,5-dimethyl-phenyl)-propylamine

HRID 1629733
ノート
印刷プレビュー

反応式

HRID 1629733 の反応式
[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([C@H:9]([NH:12][S@@](C(C)(C)C)=O)[CH2:10][CH3:11])=[CH:4][C:3]=1[CH3:19].Cl>CO>[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([C@H:9]([NH2:12])[CH2:10][CH3:11])=[CH:4][C:3]=1[CH3:19]
参加物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 313Hydrochloric AcidHCID 67346503(R)-2-Methyl-propane-2-sulfinic acid [(R)-1-(4-chloro-3,5-dimethyl-phenyl)-propyl]-amide

生成物 1

HCID 55278509(R)-1-(4-Chloro-3,5-dimethyl-phenyl)-propylamine

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A solution of intermediate INT 37 (3.4 g, 11.26 mmol) in MeOH (75 mL) was treated with HCl (4 M in dioxane, 5.63 mL, 22.53 mmol) and stirred overnight. After evaporation of the solvents, a white solid was obtained which was washed with Et2O. The solid was then dissolved in water, slightly acidified with 2 M HCl and washed with EtOAc. The aqueous layer was separated and the pH adjusted to about 11 using 2 M NaOH followed by extraction with Et2O (3×). The Et2O layers were combined, dried over sodium sulfate, filtered and concentrated.

後処理

  1. customAfter evaporation of the solvents
  2. customa white solid was obtained which
  3. washwas washed with Et2O
  4. dissolutionThe solid was then dissolved in water
  5. washwashed with EtOAc
  6. customThe aqueous layer was separated
  7. extractionfollowed by extraction with Et2O (3×)
  8. dry with materialdried over sodium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-ae478501eebb4f68a7ff21c73d12850d
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08791100B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート