Sodium sulfite heptahydrate → HCID 23704948, 화합물

HRID 346663

반응식

HRID 346663 반응식
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([S:12](Cl)(=[O:14])=[O:13])[CH:6]=[CH:5]2.O.O.O.O.O.O.O.S([O-])([O-])=O.[Na+:27].[Na+].C(=O)(O)[O-].[Na+]>O>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([S:12]([O-:14])=[O:13])[CH:6]=[CH:5]2.[Na+:27]

참가 물질

5

반응물 3

HCID 160916Sodium sulfite heptahydrateHCID 516892Sodium BicarbonateHCID 106351296-Chloronaphthalene-2-sulfonyl chloride

생성물 1

HCID 23704948HCID 23704948, 화합물수율 96.6%

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
70 °C

실험 절차

6-Chloronaphth-2-ylsulphonyl chloride (2.61 g) was added in one portion to a stirred mixture of sodium sulphite heptahydrate (4.71 g), sodium bicarbonate (1.64 g) and water (25 ml) which had been heated to 70° C. The resultant mixture was heated to that temperature for 3 hours and then allowed to cool slowly to ambient temperature. The crystalline precipitate was isolated giving sodium 6-chloronaphth-2-ylsulphinate (2.4 g) which was used without further purification.

후처리

  1. temperatureto cool slowly to ambient temperature
  2. customThe crystalline precipitate was isolated

출처 및 근거

ORD 기록
ord-479b1b54406f4419abd03e4c28b8b5b5
출처 데이터셋
uspto-grants-2007_02
특허 번호
US07173025B1

연결된 노트

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