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Hydrochloric Acid → 1-(1,2-Diamino-1-methylethyl)-1-cyclopropanecarboxylate dihydrochloride

HRID 1510343
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HRID 1510343 반응식
[NH2:1][C:2]([C:6]1([C:9]([O:11]C(C)(C)C)=[O:10])[CH2:8][CH2:7]1)([CH3:5])[CH2:3][NH2:4].O.[ClH:17]>>[ClH:17].[ClH:17].[NH2:1][C:2]([C:6]1([C:9]([OH:11])=[O:10])[CH2:7][CH2:8]1)([CH3:5])[CH2:3][NH2:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 962WaterHCID 57434367Tert-butyl 1-(1,2-diamino-1-methylethyl)-1-cyclopropanecarboxylate

생성물 1

HCID 574343681-(1,2-Diamino-1-methylethyl)-1-cyclopropanecarboxylate dihydrochloride

실험 절차

0.82 g (3.83 mmol) of the crude tert-butyl 1-(1,2-diamino-1-methyl ethyl)-1-cyclopropanecarboxylate was dissolved in concentrated hydrochloric acid (5 mL) at room temperature, and the solution was stirred at the same temperature for 30 minutes. After adding water to the reaction solution, the solvent was removed by distillation under reduced pressure. The residue was azeotropically distilled with ethanol (twice) to obtain 0.82 g (3.55 mmol, 93%) of the crude target compound as a pale yellow foam solid. The thus obtained crude product was used in the subsequent reaction with no further purification.

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후처리

  1. customthe solvent was removed by distillation under reduced pressure
  2. distillationThe residue was azeotropically distilled with ethanol (twice)
  3. customto obtain 0.82 g (3.55 mmol, 93%) of the crude target compound as a pale yellow foam solid
  4. customThe thus obtained crude product
  5. customwas used in the subsequent reaction with no further purification

출처 및 근거

ORD 기록
ord-d78f1a5a4ef64d79a5180f81b35c576e
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08211910B2

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