反応 #943989

ord-2be790c6a8a041b4bc60d9a2b9a17b3d

反応方程式

O
water
COc1cc2c(cc1O)C(=O)CCC2
7-hydroxy-6-methoxy-1-tetralone
BrCc1ccccc1
benzyl bromide
O=C([O-])[O-].[K+].[K+]
K2CO3
COc1cc2c(cc1OCc1ccccc1)C(=O)CCC2
product
収率 62.8%
COc1cc2c(cc1OCc1ccccc1)C(=O)CCC2
7-Benzyloxy-6-methoxy-3,4-dihydro-2H-naphthalen-1-one
収率 62.8%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度was heated
  2. 2
    温度to reflux overnight
  3. 3
    その他The reaction
  4. 4
    温度as cooled
  5. 5
    抽出extracted with EtOAc
  6. 6
    乾燥The EtOAc was dried over Na2SO4
  7. 7
    その他evaporated
  8. 8
    その他to give 7 g of crude product
  9. 9
    その他Crystallization with Et2O

実験手順

A mixture of 4.5 g (0.0233 mole) of 7-hydroxy-6-methoxy-1-tetralone, 5.4 g (0.032 mole) of benzyl bromide and 10 g (0.072 mole) of K2CO3 in 150 ml of acetone was heated to reflux overnight. The reaction as cooled, poured into water and extracted with EtOAc. The EtOAc was dried over Na2SO4 and evaporated to give 7 g of crude product. Crystallization with Et2O gave 4.13 g of product as a white solid, mp 110-111° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: USRE039419E1uspto-grants-2006_12