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Hydrochloric Acid → Methyl 3-aminocyclohexane-1-carboxylate

HRID 530871
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HRID 530871 반응식
C(OC([NH:8][CH:9]1[CH2:14][CH2:13][CH2:12][CH:11]([C:15]([O:17][CH3:18])=[O:16])[CH2:10]1)=O)(C)(C)C.Cl.CO>O1CCOCC1>[NH2:8][CH:9]1[CH2:14][CH2:13][CH2:12][CH:11]([C:15]([O:17][CH3:18])=[O:16])[CH2:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 59453914Methyl 3-(tert-butoxycarbonylamino)cyclohexanecarboxylate

생성물 1

HCID 13216966Methyl 3-aminocyclohexane-1-carboxylate

시약·촉매·용매 1

HCID 312751,4-Dioxane용매2회

실험 절차

In a flask, methyl 3-(tert-butoxycarbonylamino)cyclohexanecarboxylate (5.13 g, 19.94 nmol) in 1,4-dioxane (15 ml) was reacted with hydrochloric acid in dioxane (4M) (15 mL). Methanol (2 mL) was added to aid in solubility. The reaction was stirred at room temperature for 1 hour. Upon completion the reaction was concentrated, and the crude (3.86 g) was progressed to the next step without further purification.

후처리

  1. concentrationUpon completion the reaction was concentrated
  2. customthe crude (3.86 g) was progressed to the next step without further purification

출처 및 근거

ORD 기록
ord-ba9c3c9dc6bf4702a9729a199abefd56
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09351965B2

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