Water → 2,6-dichloro-N-(2-chloroethyl)benzamide

HRID 1088341ノート

反応式

HRID 1088341 の反応式
Cl.[Cl:2][CH2:3][CH2:4][NH2:5].C(=O)([O-])[O-].[K+].[K+].O.[Cl:13][C:14]1[CH:22]=[CH:21][CH:20]=[C:19]([Cl:23])[C:15]=1[C:16](Cl)=[O:17]>ClCCl>[Cl:13][C:14]1[CH:22]=[CH:21][CH:20]=[C:19]([Cl:23])[C:15]=1[C:16]([NH:5][CH2:4][CH2:3][Cl:2])=[O:17]

参加物

6

反応物 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 783922,6-Dichlorobenzoyl chlorideHCID 97937372-Chloroethylamine hydrochloride

生成物 1

HCID 150969722,6-dichloro-N-(2-chloroethyl)benzamide収率 68.8%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a stirred (vigourously) mixture of 17.4 parts of 2-chloroethanamine hydrochloride, 20.7 parts of potassium carbonate and 225 parts of water was added dropwise a mixture of 31.3 parts of 2,6-dichlorobenzoyl chloride and 120 parts of dichloromethane at room temperature: slightly exothermic reaction. Upon completion, stirring at room temperature was continued for one hour. The organic phase was separated and the aqueous phase was extracted with dichloromethane. The combined organic phases were washed with water, dried, filtered and evaporated. The residue was crystallized from methylbenzene. The product was filtered off and dried, yielding 25.8 parts (68.8%) of 2,6-dichloro-N-(2-chloroethyl)benzamide; mp. 113.8° C. (intermediate 30).

後処理

  1. additionwas added dropwise
  2. customslightly exothermic reaction
  3. stirringUpon completion, stirring at room temperature
  4. customThe organic phase was separated
  5. extractionthe aqueous phase was extracted with dichloromethane
  6. washThe combined organic phases were washed with water
  7. customdried
  8. filtrationfiltered
  9. customevaporated
  10. customThe residue was crystallized from methylbenzene
  11. filtrationThe product was filtered off
  12. customdried

出典と根拠

ORDレコード
ord-b90cb27282c6471eaa352cb74f4e6f51
出典データセット
uspto-grants-1990_10
特許番号
US04962115

反応ノート

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