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1-tert-Butyl 4-ethyl 4-methylpiperidine-1,4-dicarboxylate → Ethyl 4-methylpiperidine-4-carboxylate hydrochloride

HRID 712160
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HRID 712160 반응식
[CH3:1][C:2]1([C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH2:7][CH2:6][N:5](C(OC(C)(C)C)=O)[CH2:4][CH2:3]1.[ClH:20].O1CCOCC1>O1CCOCC1>[ClH:20].[CH3:1][C:2]1([C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1
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참가 물질

4

반응물 2

HCID 162182761-tert-Butyl 4-ethyl 4-methylpiperidine-1,4-dicarboxylateHCID 204431481,4-Dioxane hydrochloride

생성물 1

HCID 19361804Ethyl 4-methylpiperidine-4-carboxylate hydrochloride

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

To an ice-cold solution of O1-tert-butyl O4-ethyl 4-methylpiperidine-1,4-dicarboxylate (1 g, 3.68 mmol) in 1,4-dioxane (10 mL) was added HCl-1,4-dioxane (4.0 M, 15 mL) solution. The mixture was stirred at rt for 30 minutes. After completion of reaction (by TLC), solvent was evaporated to obtain brown solid material (0.90 g) that was carried forward to the next step without purification. MS: 172.16 [M+H]+.

후처리

  1. customAfter completion of reaction (by TLC), solvent
  2. customwas evaporated

출처 및 근거

ORD 기록
ord-299fe4dfdfa74898a0516eeaf7e186e2
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181234B2

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