tert-Butyl 4-oxopiperidine-1-carboxylate → 1-tert-Butyloxycarbonyl-3-bromo-4-oxopiperidine

HRID 12061

反応式

HRID 12061 の反応式
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][C:11](=[O:14])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[Br:15]C1CC(C(C)C)CCC1=O>>[C:1]([O:5][C:6]([N:8]1[CH2:9][CH2:10][C:11](=[O:14])[CH:12]([Br:15])[CH2:13]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]

参加物

3

反応物 2

HCID 735900tert-Butyl 4-oxopiperidine-1-carboxylateHCID 627080672-Bromo-4-isopropyl-cyclohexanone

生成物 1

HCID 106839701-tert-Butyloxycarbonyl-3-bromo-4-oxopiperidine

実験手順

The bromination of 4-oxo-piperidine-1-carboxylic acid tert-butyl ester takes place in a manner similar to that described above for the preparation of 2-bromo-4-isopropyl-cyclohexanone. The title compound is reacted as a crude product without further characterization.

出典と根拠

ORDレコード
ord-0f91e36356c443afb325cec8d55ab4f8
出典データセット
uspto-grants-2010_06
特許番号
US07727979B2

関連ノート

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