Реакция #93567

ord-c80d1a5254c34b05b04ee0370dcfcba0

Уравнение реакции

O=S([O-])S(=O)(=O)[O-].[Na+].[Na+]
sodium metabisulphite
CC(=O)OO
Peracetic acid
CC(=O)[O-].[Na+]
sodium acetate
C1=CCC(Cc2ccc(-c3ccccc3)cc2)C1
4-(3-cyclopenten-1-ylmethyl)-1,1'-biphenyl
c1ccc(-c2ccc(CC3CC4OC4C3)cc2)cc1
products
c1ccc(-c2ccc(CC3CC4OC4C3)cc2)cc1
3-([1,1'-biphenyl]-4-ylmethyl)-6-oxabicyclo [3.1.0]hexane

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураit was cooled
  2. 2
    ПромывкаThe chloroform layer was washed with water, dilute sodium hydroxide solution, water and brine
  3. 3
    Другоеdried
  4. 4
    Другоеevaporated

Методика

Peracetic acid in acetic acid (60 ml; 40%) was added over 5 min. to a cooled mixture of sodium acetate (8g) and 4-(3-cyclopenten-1-ylmethyl)-1,1'-biphenyl (20 g) in chloroform (150 ml). The mixture was stirred vigorously at room temperature for 4 h., then it was cooled and a solution of sodium metabisulphite was slowly added. The chloroform layer was washed with water, dilute sodium hydroxide solution, water and brine, dried and evaporated to give a 1:3 mixture (TLC) of two products (20 g). Crystallisation from methylene dichloride-ether gave two crops, rich in the slower running isomer (TLC). Recrystallisation from methylene dichloride/ether gave pure (±)-(1α,3α,5α)-3-([1,1'-biphenyl]-4-ylmethyl)-6-oxabicyclo[3.1.0]hexane (9.6 g), m.p. 130°-132° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04613619uspto-grants-1986_09