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Ethyl bromoacetate → 1-(2-Ethoxy-2-oxoethyl)-1-ethylpiperidin-1-ium bromide

HRID 1897535
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HRID 1897535 반응식
[CH2:1]([N:3]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1)[CH3:2].[CH2:9]([O:11][C:12](=[O:15])[CH2:13][Br:14])[CH3:10]>ClCCl>[Br-:14].[CH2:9]([O:11][C:12](=[O:15])[CH2:13][N+:3]1([CH2:1][CH3:2])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1)[CH3:10]
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참가 물질

4

반응물 2

HCID 7748Ethyl bromoacetateHCID 13007N-Ethylpiperidine

생성물 1

HCID 30482831-(2-Ethoxy-2-oxoethyl)-1-ethylpiperidin-1-ium bromide수율 98.6%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 1-ethylpiperidine (2.5 g, 22.1 mmol) in dichloromethane (4 mL) was added ethylbromoacetate (3.7 g, 22.1 mmol) via a syringe. The mixture was stirred at room temperature overnight. The resulting white precipitate was washed with hexane and ethylacetate to give 6.1 g, 98.6% yield of the product as a white solid. Positive mode ESI/MS: m/z=200.4 (M+, minus Br); confirmed by 1H NMR.

후처리

  1. washThe resulting white precipitate was washed with hexane and ethylacetate

출처 및 근거

ORD 기록
ord-b4686a9f058d409caf8bc5ca5987b92d
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08519125B2

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