反应 #56590

ord-7f83b244a5014c8fbe2f48fda79a83a5

反应方程式

ClCCCCCCOC1CCCCO1
2-(6-chlorohexyloxy)tetrahydropyrane
Oc1ccc(O)cc1
hydroquinone
O=C([O-])[O-].[K+].[K+]
potassiumcarbonate
[I-].[K+]
potassiumiodide
Oc1ccc(OCCCCCCOC2CCCCO2)cc1
product
收率 82.5%
Oc1ccc(OCCCCCCOC2CCCCO2)cc1
4-(6-(2-Tetrahydropyranyl)oxyhexyloxy)phenol
收率 82.5%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他to react for 4 days at 80° C
  2. 2
    萃取extracted with ether
  3. 3
    干燥The organic phase was then dried over sodium sulphate
  4. 4
    过滤filtered
  5. 5
    浓缩concentrated to dryness

实验过程

A mixture of 10 g of 2-(6-chlorohexyloxy)tetrahydropyrane, 25 g of hydroquinone, 31 g of potassiumcarbonate, 0.752 g of potassiumiodide and 250 ml of dimethylsulfoxide was allowed to react for 4 days at 80° C. Subsequently, the reaction mixture was cooled to room temperature and after addition of water extracted with ether. The organic phase was then dried over sodium sulphate, filtered and concentrated to dryness. Chromatography on silica with 10% ethylacetate in toluene gave 11 g of product as a yellowish oil.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07419620B2uspto-grants-2008_09