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Gamma-Butyrolactone → 4-Hydroxy-1-(2-naphthyl)-1-butanone

HRID 2229250
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HRID 2229250 반응식
Br[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=1.[Li]CCCC.[C:17]1(=[O:22])[O:21][CH2:20][CH2:19][CH2:18]1.[NH4+].[Cl-]>C1COCC1.CCCCCC>[OH:22][CH2:17][CH2:18][CH2:19][C:20]([C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=1)=[O:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 7302Gamma-ButyrolactoneHCID 113722-BromonaphthaleneHCID 25517Ammonium ChlorideHCID 178418339Butyllithium

생성물 1

HCID 184670444-Hydroxy-1-(2-naphthyl)-1-butanone

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매
HCID 8058
Hexane
용매

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온도
-78 °C

실험 절차

To a cooled (−78° C.) solution of 2-bromonaphthalene (10.77 g) in THF (150 ml) was added n-BuLi in hexane (1.65M, 36 ml) and the mixture was stirred at −78° C. for 30 minutes. To the solution was added γ-butyrolactone (25 ml) and the mixture was stirred at −78° C. for 1 minute. Aqueous solution of NH4Cl was added and the mixture was extracted with ethyl acetate. The extract was washed with aqueous NH4Cl solution, water and brine, dried and concentrated. The residue was chromatographed on silica gel (hexane:ethyl acetate=3:1) followed by recrystallization from cyclohexane-ethyl acetate to give the titled compound (6.71 g) as a colorless solid.

후처리

  1. stirringthe mixture was stirred at −78° C. for 1 minute
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe extract was washed with aqueous NH4Cl solution, water and brine
  4. customdried
  5. concentrationconcentrated
  6. customThe residue was chromatographed on silica gel (hexane:ethyl acetate=3:1)
  7. customfollowed by recrystallization from cyclohexane-ethyl acetate

출처 및 근거

ORD 기록
ord-3a2a7b57dbe9461c8a11e1ab97deb6dc
출처 데이터셋
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06420375B1

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