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Hydrochloric Acid → 2-(Methanesulfonyl)benzylamine hydrochloride

HRID 1819494
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HRID 1819494 반응식
C(OC(=O)[NH:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[S:15]([CH3:18])(=[O:17])=[O:16])(C)(C)C.[ClH:20]>O1CCOCC1.C(Cl)(Cl)Cl>[ClH:20].[CH3:18][S:15]([C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=1[CH2:8][NH2:7])(=[O:16])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 22464527(2-Methanesulfonyl-benzyl)-carbamic acid tert-butyl ester

생성물 1

HCID 162183342-(Methanesulfonyl)benzylamine hydrochloride수율 89.3%

시약·촉매·용매 2

HCID 6212Chloroform용매HCID 312751,4-Dioxane용매

실험 절차

(2-Methanesulfonyl-benzyl)-carbamic acid tert-butyl ester (1.55 g, 5.43 mmol) was dissolved in warm dioxane (50 mL) and cooled to room temperature. HCl solution (4M solution in dioxane, 20 ml, 80 mmol) was added. After 20 h, a white precipitate had formed. The reaction was diluted with CHCl3 (50 mL) and filtered. The white solid was washed with CHCl3 and dried in-vacuo to yield 1.075g of 2-methanesulfonyl-benzylamine hydrochloride as an off white solid, m/z 186.6 (M+1)+.

후처리

  1. customa white precipitate had formed
  2. filtrationfiltered
  3. washThe white solid was washed with CHCl3
  4. customdried in-vacuo

출처 및 근거

ORD 기록
ord-9a10e61025534704825a2a2dc82d2516
출처 데이터셋
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07601714B2

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