tert-butyl (2S)-2-methyl-4-oxopiperidine-1-carboxylate → (2S)-Tert-butyl 4-allyl-4-hydroxy-2-methylpiperidine-1-carboxylate

HRID 403506노트

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HRID 403506 반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][C:11](=[O:14])[CH2:10][C@@H:9]1[CH3:15])=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH2:16]([Mg]Br)[CH:17]=[CH2:18]>CCOCC>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][C:11]([CH2:18][CH:17]=[CH2:16])([OH:14])[CH2:10][C@@H:9]1[CH3:15])=[O:7])([CH3:4])([CH3:2])[CH3:3]

참가 물질

4

반응물 2

HCID 11401606tert-butyl (2S)-2-methyl-4-oxopiperidine-1-carboxylateHCID 178455850HCID 178455850, 화합물

생성물 1

HCID 68379051(2S)-Tert-butyl 4-allyl-4-hydroxy-2-methylpiperidine-1-carboxylate

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

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온도
0 °C

실험 절차

In a argon flushed dry 25 ml 2-neckoundbottomflask (S)-2-methyl-4-oxo-piperidine-1-carboxylic acid tert-butyl ester (34) (0.6 g, 2.81 mmol) was dissolved in 10 ml of ether. A 1M solution of allylmagnesiumbromide in Et2O (3.66 ml, 3.66 mmol) was added dropwise at 0° C. The reaction mixture was stirred at 0° C. for 2 h. The mixture was quenched with NH4Cl solution and extracted with ether. The organic layer was washed with brine, dried over Na2 SO4 and evaporated. The crude product was purified by flash chromatography (silica gel, 20-30% EtOAc/cyclohexane) which furnished the product as white solid

후처리

  1. customIn a argon flushed
  2. customThe mixture was quenched with NH4Cl solution
  3. extractionextracted with ether
  4. washThe organic layer was washed with brine
  5. customdried over Na2 SO4
  6. customevaporated
  7. customThe crude product was purified by flash chromatography (silica gel, 20-30% EtOAc/cyclohexane) which

출처 및 근거

ORD 기록
ord-821fde4c95414ddb8f3cf416e7d0b7fa
출처 데이터셋
uspto-grants-2014_06
특허 번호
US08748435B2

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