反应 #1702064

ord-2ccb158dc8244890a8d5a71e3e4e8d4b

反应方程式

CC1(C)CCC(C)(C)c2cc(O)ccc21
5,6,7,8-tetrahydro-2-hydroxy-5,5,8,8-tetramethylnaphthalene
ClCCl
dichloromethane
[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
CCC(=O)Cl
propionyl chloride
CCC(=O)c1cc2c(cc1O)C(C)(C)CCC2(C)C
5,6,7,8-tetrahydro-3-hydroxy-5,5,8,8-tetramethyl-2-naphthyl ethyl ketone

溶剂

反应条件

温度
60°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    萃取extracted by ethyl acetate
  2. 2
    洗涤The organic layer was washed by water
  3. 3
    干燥a saturated sodium hydrogen carbonate aq. solution, and a saturated saline solution, dried over magnesium sulfate
  4. 4
    浓缩concentrated under reduced pressure
  5. 5
    其他The crude product was purified by silica gel column chromatography

实验过程

To 5,6,7,8-tetrahydro-2-hydroxy-5,5,8,8-tetramethylnaphthalene (204 mg, 1.00 mmol) were added anhydrous dichloromethane (1 mL), aluminum chloride (148 mg, 1.12 mmol), and propionyl chloride (101.7 mg, 1.10 mmol) followed by stirring at 60° C. for 16 hours. The reaction solution was poured into cold water and extracted by ethyl acetate. The organic layer was washed by water, a saturated sodium hydrogen carbonate aq. solution, and a saturated saline solution, dried over magnesium sulfate, and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography using hexane/ethyl acetate (20/1) as an elution solvent. The yield was 117 mg (45%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08765719B2uspto-grants-2014_07