反应 #943989

ord-2be790c6a8a041b4bc60d9a2b9a17b3d

反应方程式

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
收率 62.8%
COc1cc2c(cc1OCc1ccccc1)C(=O)CCC2
7-Benzyloxy-6-methoxy-3,4-dihydro-2H-naphthalen-1-one
收率 62.8%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

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

实验过程

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.

来源

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