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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Butyl bromide → HCID 68485070, 화합물

HRID 1896973
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HRID 1896973 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:8]([C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[CH2:9][NH2:10])[CH:5]=[CH:6][CH:7]=1.C([O-])([O-])=O.[K+].[K+].Br[CH2:25][CH2:26][CH2:27][CH3:28]>CC(C)=O>[CH2:25]([O:1][C:2]1[CH:3]=[C:4]([CH:8]([C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[CH2:9][NH2:10])[CH:5]=[CH:6][CH:7]=1)[CH2:26][CH2:27][CH3:28]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8002Butyl bromideHCID 11430Potassium CarbonateHCID 68485743HCID 68485743, 화합물

생성물 1

HCID 68485070HCID 68485070, 화합물

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a solution in acetone (240 ml), of 2-(3-hydroxyphenyl)-(tert-butoxycarbonyl)ethylamine obtained in Step 1, K2CO3 (19.8 g) and 1-bromobutane (15 ml) were added. The suspension was refluxed for 3 days and the solvent was evaporated under reduced pressure. The residue was dissolved in H2O (200 ml) and extracted with CH2Cl2 (2×200 ml). The solvent was eliminated under reduced pressure and the residue was purified by flash chromatography (petroleum ether/EtOAc 85:15) affording 1 (11.3 g, 81% over 3 steps) of the title compound as colorless oil.

후처리

  1. temperatureThe suspension was refluxed for 3 days
  2. customthe solvent was evaporated under reduced pressure
  3. dissolutionThe residue was dissolved in H2O (200 ml)
  4. extractionextracted with CH2Cl2 (2×200 ml)
  5. customthe residue was purified by flash chromatography (petroleum ether/EtOAc 85:15)

출처 및 근거

ORD 기록
ord-982a0896c5c44837981359e721fcf6c8
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08519000B2

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