Реакция #409239

ord-b70296b47fef4bb4ba62f871f81db572

Уравнение реакции

C(=NC1CCCCC1)=NC1CCCCC1
dicyclohexylcarbodiimide
COCc1cc(-c2c(S(C)(=O)=O)ccc(C(=O)O)c2Cl)no1
2-chloro-3-(5-methoxymethylisoxazol-3-yl)-4-methylsulfonylbenzoic acid
O=C1CCCCC1=O
cyclohexanedione
COCc1cc(-c2c(S(C)(=O)=O)ccc(C(=O)OC3=CC(=O)CCC3)c2Cl)no1
3-Oxo-1-cyclohexenyl 2-chloro-3-(5-methoxymethylisoxazol-3-yl)-4-methylsulfonylbenzoate

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Фильтрацияthe precipitate is filtered off with suction
  2. 2
    Промывкаthe filtrate is washed with water
  3. 3
    ДругоеAfter the removal of the solvent, 1.22 g (92% of theory) of 3-oxo-1-cyclohexenyl 2-chloro-3-(5-methoxymethylisoxazol-3 yl)-4-methyl-sulfonylbenzoate
  4. 4
    Другоеare obtained as a yellowish, partly crystalline oil

Методика

1.04 g (3.0 mmol) of 2-chloro-3-(5-methoxymethylisoxazol-3-yl)-4-methylsulfonylbenzoic acid are introduced into 50 ml of dichloromethane together with 0.37 g (3.3 mmol) of cyclohexanedione and treated with 0.68 g (3.3 mmol) of dicyclohexylcarbodiimide. After stirring at room temperature for 16 hours, the precipitate is filtered off with suction and the filtrate is washed with water. After the removal of the solvent, 1.22 g (92% of theory) of 3-oxo-1-cyclohexenyl 2-chloro-3-(5-methoxymethylisoxazol-3 yl)-4-methyl-sulfonylbenzoate are obtained as a yellowish, partly crystalline oil.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06211216B1uspto-grants-2001_04