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HRID1107450

反应详情

EQUATION

反应方程式

HRID 1107450 的结构方程式

REACTANTS

反应物

15
结构：O=C(O)c1ccc(Cl)cc1
HCID6318

4-Chlorobenzoic acid

C7H5ClO2

结构：O=C(O)c1ccc2ccccc2c1
HCID7123

2-Naphthalenecarboxylic acid

C11H8O2

结构：O=C(O)c1ccc2c(c1)OCO2
HCID7196

1,3-Benzodioxole-5-carboxylic acid

C8H6O4

结构：O=C(Cl)c1ccccc1
HCID7412

Benzoyl chloride

C7H5ClO

结构：COc1cc(C(=O)O)cc(OC)c1OC
HCID8357

3,4,5-Trimethoxybenzoic acid

C10H12O5

结构：O=C(O)c1cccc(C(F)(F)F)c1
HCID9963

3-(Trifluoromethyl)benzoic acid

C8H5F3O2

结构：CC(C(=O)O)c1ccccc1
HCID10296

(+/-)-2-Phenylpropionic acid

C9H10O2

结构：COc1cccc(C(=O)O)c1
HCID11461

Benzoic acid, 3-methoxy-

C8H8O3

结构：CN(C)c1cccc(C(=O)O)c1
HCID66837

Benzoic acid, 3-(dimethylamino)-

C9H11NO2

结构：CS(=O)(=O)c1ccc(C(=O)O)cc1
HCID77670

p-(Methylsulphonyl)benzoic acid

C8H8O4S

结构：O=C(O)c1cc(F)cc(F)c1
HCID101265

Benzoic acid, 3,5-difluoro-

C7H4F2O2

结构：COc1ccc2cc(C(=O)O)ccc2c1
HCID349181

6-Methoxy-2-naphthoic acid

C12H10O3

结构：CS(=O)c1ccc(C(=O)O)cc1
HCID4961892

4-(methylsulfinyl)benzoic acid

C8H8O3S

结构：CC(C(=O)O)c1ccc2c(c1)OCO2
HCID18399654

未命名化合物

结构：CN(C)c1cc(C(=O)O)cc2ccccc12
HCID21188426

未命名化合物

PRODUCTS

生成物

1
结构：O=C(CS(=O)(=O)c1ccccc1)c1ccccc1
HCID76949

1-Phenyl-2-(phenylsulphonyl)ethan-1-one

C14H12O3S

PROCEDURE

实验过程

When the acid chloride of 4-chlorobenzoic acid, 3-methoxybenzoic acid, 3,4-methylenedioxybenzoic acid, 3,4,5-trimethoxybenzoic acid, 3-trifluoromethylbenzoic acid, 3-dimethylaminobenzoic acid, 4-methylthiobenzoic, 4-methylsulfinylbenzoic acid, 4methylsulfonylbenzoic acid, 3,5-difluorobenzoic acid, 2-naphthoic acid, 4-dimethylamino-2-naphthoic acid, 6-methoxy-2-naphthoic acid, 2-phenylpropionic acid and 2-(3,4-methylenedioxyphenyl) propionic acid are used in place of benzoyl chloride above, the corresponding substituted ketosulfones are prepared.

WORKUP

后处理

  1. customare prepared