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

HRID 1851884
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반응식

HRID 1851884 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 71074743(R)-N-((S)-1-(4-(tert-butyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide

생성물 1

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

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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]+

후처리

  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

출처 및 근거

ORD 기록
ord-64b6db82b7824ced9eae095d8db5da56
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08957093B2

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