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Hydrochloric Acid → 4-(2-(Methylsulfonyl)phenoxy)piperidine hydrochloride

HRID 522859
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반응식

HRID 522859 반응식
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([O:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[S:21]([CH3:24])(=[O:23])=[O:22])[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:25]>O1CCOCC1>[ClH:25].[CH3:24][S:21]([C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=1[O:14][CH:11]1[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]1)(=[O:23])=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 67355788Tert-butyl 4-(2-(methylsulfonyl)phenoxy)piperidine-1-carboxylate

생성물 1

HCID 665924674-(2-(Methylsulfonyl)phenoxy)piperidine hydrochloride수율 80.7%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

To 4-(2-methanesulfonyl-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester (2.6 g, 7.3 mmol) was added HCl in dioxane solution (4M) (15 mL). The reaction mixture was stirred at RT for 5 h. After completion of the reaction (monitored by TLC), the excess dioxane was removed in vacuo affording an off white solid. The crude material was washed with diethyl ether (3×20 mL) to afford 4-(2-(methylsulfonyl)phenoxy)piperidine hydrochloride (1.3 g, 80.7%).

후처리

  1. customAfter completion of the reaction (monitored by TLC)
  2. customthe excess dioxane was removed in vacuo
  3. customaffording an off white solid
  4. washThe crude material was washed with diethyl ether (3×20 mL)

출처 및 근거

ORD 기록
ord-ae5dad731a6b4f99be29dcc4946abd12
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09334269B2

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