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Allyl bromide → 4-Allyloxy-2,2,6,6-tetramethylpiperidine hydrobromide

HRID 434456
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인쇄 미리보기

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HRID 434456 반응식
[CH2:1]([O:4][CH:5]1[CH2:10][C:9]([CH3:12])([CH3:11])[NH:8][C:7]([CH3:14])([CH3:13])[CH2:6]1)[CH:2]=[CH2:3].C([Br:18])C=C>CCOCC>[BrH:18].[CH2:1]([O:4][CH:5]1[CH2:6][C:7]([CH3:14])([CH3:13])[NH:8][C:9]([CH3:12])([CH3:11])[CH2:10]1)[CH:2]=[CH2:3]
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참가 물질

4

반응물 2

HCID 7841Allyl bromideHCID 11117001Piperidine, 2,2,6,6-tetramethyl-4-(2-propen-1-yloxy)-

생성물 1

HCID 197362214-Allyloxy-2,2,6,6-tetramethylpiperidine hydrobromide

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

반응 조건

온도
90 °C

실험 절차

A mixture of 9.87 parts of 4-allyloxy-2,2,6,6-tetramethylpiperidine and 3.03 parts of allyl bromide was heated at 90° C. for 96 hours. Ether was added to the cooled reaction mixture and the 4-allyloxy-2,2,6,6-tetramethylpiperidine hydrobromide formed during the reaction was filtered off. The ether solvent was removed by distillation under reduced pressure and the residue purified by chromatography to give 4-allyloxy-1-allyl-2,2,6,6-tetramethylpiperidine.

출처 및 근거

ORD 기록
ord-0c351d6a7d784c47934264b374a5a013
출처 데이터셋
uspto-grants-1983_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
USRE031343

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