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Hydrochloric Acid → (1S)-1-Benzyl-2-(benzyloxy)ethylamine hydrochloride

HRID 2297703
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인쇄 미리보기

반응식

HRID 2297703 반응식
[CH2:1]([C@H:8]([NH2:25])[CH:9](C(OC(C)(C)C)=O)[O:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[ClH:26]>CO>[ClH:26].[CH2:1]([C@H:8]([NH2:25])[CH2:9][O:10][CH2:11][C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 69931105(1S)-1-Benzyl-2-(benzyloxy)-N-(t-butoxycarbonyl)ethylamine

생성물 1

HCID 12815229(1S)-1-Benzyl-2-(benzyloxy)ethylamine hydrochloride수율 99%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

(1S)-1-Benzyl-2-(benzyloxy)-N-(t-butoxycarbonyl)ethylamine (205 mg) is dissolved in a 2.3 N solution of hydrogen chloride in methanol (3 ml), and the solution is stirred for one hour. The reaction mixture is concentrated under reduced pressure, ether is added to the concentrate, and the resulting precipitate is filtered off to give 143 mg (99%) of the titled compound (Reference compound No. 12-1) as crystals.

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후처리

  1. concentrationThe reaction mixture is concentrated under reduced pressure, ether
  2. additionis added to the concentrate
  3. filtrationthe resulting precipitate is filtered off

출처 및 근거

ORD 기록
ord-7e881df1e9184954b7f8176c65970fea
출처 데이터셋
uspto-grants-2002_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06492370B1

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