反応 #2075010

ord-be28c555b33947a68fa454b43186ba49

反応方程式

O=C1OCCC1Br
3-bromo-dihydrofuran-2(3H)-one
OCc1ccc(S)cc1
(4-mercaptophenyl)methanol
CCN(CC)CC
triethylamine
O=C1OCCC1Sc1ccc(CO)cc1
product
収率 73.3%
O=C1OCCC1Sc1ccc(CO)cc1
3-(4-(hydroxymethyl)phenylthio)dihydrofuran-2(3H)-one
収率 73.3%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    洗浄washed sequentially with saturated NH4Cl and NaCl solutions
  2. 2
    乾燥The organics were dried over MgSO4
  3. 3
    濃縮concentrated under reduced pressure

実験手順

3-bromo-dihydrofuran-2(3H)-one (2.35 g, 14.3 mmol) was added to a solution of (4-mercaptophenyl)methanol (2.00 g, 14.0 mmol) and triethylamine (2.4 mmol, 17 mmol). The reaction was stirred at room temperature overnight, then was diluted with CH2Cl2 and washed sequentially with saturated NH4Cl and NaCl solutions. The organics were dried over MgSO4 and concentrated under reduced pressure to provide the product as a viscous oil (2.3 g, 72%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07553842B2uspto-grants-2009_06