反応 #56590

ord-7f83b244a5014c8fbe2f48fda79a83a5

反応方程式

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

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他to react for 4 days at 80° C
  2. 2
    抽出extracted with ether
  3. 3
    乾燥The organic phase was then dried over sodium sulphate
  4. 4
    ろ過filtered
  5. 5
    濃縮concentrated to dryness

実験手順

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.

出典

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