反応 #450284

ord-080364f263cb406e8277d0c2abcbe9af

反応方程式

O=C(Oc1ccc(O)cc1)c1ccccc1
4-hydroxyphenyl benzoate
O=C([O-])[O-].[K+].[K+]
potassium carbonate
ClCC=C(Cl)Cl
1,1,3-trichloropropene
CN(C)C=O
N,N-dimethylformamide
O=C(Oc1ccc(OCC=C(Cl)Cl)cc1)c1ccccc1
4-(3,3-dichloro-2-propenyloxy)phenyl benzoate
収率 96.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出extracted twice with 150 ml of diethyl ether
  2. 2
    洗浄The combined ether layer was washed with water
  3. 3
    乾燥dried with anhydrous magnesium sulfate
  4. 4
    濃縮concentrated
  5. 5
    その他to obtain a crude product

実験手順

A reaction vessel was charged with 30.5 g of 4-hydroxyphenyl benzoate, 21.6 g of potassium carbonate, 20.8 g of 1,1,3-trichloropropene and 100 ml of N,N-dimethylformamide. After stirring at room temperature for 15 hours, the reaction mixture was poured into water, and extracted twice with 150 ml of diethyl ether. The combined ether layer was washed with water, dried with anhydrous magnesium sulfate, and concentrated to obtain a crude product. The crude product was subjected to silica gel chromatography, which afforded 44.1 g of 4-(3,3-dichloro-2-propenyloxy)phenyl benzoate (96% yield).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05872137uspto-grants-1999_02