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Hydrochloric Acid → (S)-1-(4-(tert-butyl)phenyl)ethanaminium chloride

HRID 1851884
ノート
印刷プレビュー

反応式

HRID 1851884 の反応式
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([C@@H:11]([NH:13][S@@](C(C)(C)C)=O)[CH3:12])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[ClH:20]>CO>[Cl-:20].[C:1]([C:5]1[CH:6]=[CH:7][C:8]([C@@H:11]([NH3+:13])[CH3:12])=[CH:9][CH:10]=1)([CH3:4])([CH3:2])[CH3:3]
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 71074743(R)-N-((S)-1-(4-(tert-butyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide

生成物 1

HCID 86674539(S)-1-(4-(tert-butyl)phenyl)ethanaminium chloride

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of (R)—N—((S)-1-(4-(tert-butyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide (977 mg) in MeOH (1.75 mL) was added conc. HCl (1.75 mL). The reaction was aged at room temperature monitoring disappearance of starting material by analytical reverse-phase HPLC. When the starting material was consumed, the reaction was concentrated in vacuo. The crude residue was resuspended in MeOH (1 mL) and crashed out of solution by the addition of Et2O. Filtration afforded the title compound as a colorless solid (559 mg). ESI-MS (m/z): 161 [M+H—NH3]+, 338 [2M+H—NH3]+

後処理

  1. customwas aged at room temperature
  2. customWhen the starting material was consumed
  3. concentrationthe reaction was concentrated in vacuo
  4. additioncrashed out of solution by the addition of Et2O
  5. filtrationFiltration

出典と根拠

ORDレコード
ord-64b6db82b7824ced9eae095d8db5da56
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08957093B2

反応ノート

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