3-Bromopentane → N-(4-(2-ethyl-1-hydroxybutyl)phenyl)acetamide

HRID 1271317노트

반응식

HRID 1271317 반응식
Br[CH:2]([CH2:5][CH3:6])[CH2:3][CH3:4].[Mg].[CH:8]([C:10]1[CH:15]=[CH:14][C:13]([NH:16][C:17](=[O:19])[CH3:18])=[CH:12][CH:11]=1)=[O:9].[NH4+].[Cl-]>CCOCC.C1COCC1>[CH2:3]([CH:2]([CH2:5][CH3:6])[CH:8]([C:10]1[CH:11]=[CH:12][C:13]([NH:16][C:17](=[O:19])[CH3:18])=[CH:14][CH:15]=1)[OH:9])[CH3:4]

참가 물질

7

반응물 4

HCID 157383-BromopentaneHCID 25517Ammonium ChlorideHCID 739424-AcetamidobenzaldehydeHCID 5462224Magnesium

생성물 1

HCID 22603035N-(4-(2-ethyl-1-hydroxybutyl)phenyl)acetamide수율 52.2%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매2회HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 3-bromopentane (0.331 mol) in (C2H5)2O (200 ml) was added dropwise to a solution of magnesium turnings (0.331 mol) in (C2H5)2O, the mixture was stirred at RT for 2 hours and then cooled to 0° C. A solution of N-(4-formylphenyl)acetamide (0.11 mol) in THF (400 ml) was added dropwise and the mixture was stirred for 10 minutes. The mixture was poured into aqueous NH4Cl and extracted with EtOAc. The organic layer was dried, filtered off and the solvent evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 97/3/0.1). The pure fractions were collected and evaporated, yielding 13.5 g (52%) of (±)-N-[4-(2-ethyl-1-hydroxybutyl)phenyl]acetamide (interm. 13).

후처리

  1. temperaturecooled to 0° C
  2. stirringthe mixture was stirred for 10 minutes
  3. extractionextracted with EtOAc
  4. customThe organic layer was dried
  5. filtrationfiltered off
  6. customthe solvent evaporated
  7. customThe residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 97/3/0.1)
  8. customThe pure fractions were collected
  9. customevaporated

출처 및 근거

ORD 기록
ord-90738b8ececc47f5b70cef8d76539038
출처 데이터셋
uspto-grants-2007_04
특허 번호
US07205312B2

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