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

HRID 2229250
ノート
印刷プレビュー

反応式

HRID 2229250 の反応式
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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒
HCID 8058
Hexane
溶媒

反応条件

温度
-78 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-3a2a7b57dbe9461c8a11e1ab97deb6dc
出典データセット
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06420375B1

反応ノート

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