Thionyl Chloride → 7-Methylsulfamoyl-1,4-benzodioxane-5-carbonyl chloride

HRID 1413135

반응식

HRID 1413135 반응식
S(Cl)([Cl:3])=O.[CH3:5][NH:6][S:7]([C:10]1[CH:11]=[C:12]([C:20]([OH:22])=O)[C:13]2[O:18][CH2:17][CH2:16][O:15][C:14]=2[CH:19]=1)(=[O:9])=[O:8]>C(Cl)(Cl)Cl>[CH3:5][NH:6][S:7]([C:10]1[CH:11]=[C:12]([C:20]([Cl:3])=[O:22])[C:13]2[O:18][CH2:17][CH2:16][O:15][C:14]=2[CH:19]=1)(=[O:9])=[O:8]

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 64553172,3-Dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxylic acid

생성물 1

HCID 205447207-Methylsulfamoyl-1,4-benzodioxane-5-carbonyl chloride

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

176.5 g of thionyl chloride were introduced into a balloon flask provided with a condenser. Then, in portions, 135 g of 7-methylsulfamoyl-1,4-benzodioxane-5-carboxylic acid were added under heating at 40°-45° C. The mixture was heated under reflux and then treated with 250 cm3 chloroform. The precipitate was dried off and washed with chloroform.

후처리

  1. customprovided with a condenser
  2. temperatureunder heating at 40°-45° C
  3. temperatureThe mixture was heated
  4. temperatureunder reflux
  5. customThe precipitate was dried off
  6. washwashed with chloroform

출처 및 근거

ORD 기록
ord-a10e87002b2249df8567e7a151277391
출처 데이터셋
uspto-grants-1981_02
특허 번호
US04248885

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