p-Toluenesulfonic acid → Antimony tris(p-toluene sulfonate)

HRID 444371

반응식

HRID 444371 반응식
[Sb:1](Cl)(Cl)Cl.[C:5]1([CH3:15])[CH:10]=[CH:9][C:8]([S:11]([OH:14])(=[O:13])=[O:12])=[CH:7][CH:6]=1.O.[C:17]1([CH3:27])[CH:22]=[CH:21][C:20]([S:23]([OH:26])(=[O:25])=[O:24])=[CH:19][CH:18]=1.[Sb]>C1(C)C=CC=CC=1.O>[C:5]1([CH3:15])[CH:6]=[CH:7][C:8]([S:11]([O-:14])(=[O:12])=[O:13])=[CH:9][CH:10]=1.[C:17]1([CH3:27])[CH:18]=[CH:19][C:20]([S:23]([O-:26])(=[O:24])=[O:25])=[CH:21][CH:22]=1.[C:5]1([CH3:15])[CH:6]=[CH:7][C:8]([S:11]([O-:14])(=[O:12])=[O:13])=[CH:9][CH:10]=1.[Sb+3:1]

참가 물질

7

반응물 4

HCID 6101p-Toluenesulfonic acidHCID 24814Antimony trichloride2회HCID 521998p-Toluenesulfonic acid monohydrateHCID 5354495Antimony

생성물 1

HCID 86736930Antimony tris(p-toluene sulfonate)

시약·촉매·용매 2

HCID 962Water용매HCID 1140Toluene용매2회

실험 절차

This compound was prepared by a double decomposition reaction between antimony trichloride and p-toluene sulfonic acid. A solution of 28.53 g (0.15 mole) of p-toluene sulfonic acid monohydrate in 150 cc of toluene was distilled until the water was removed. The anhydrous acid solution was then added dropwise to a solution of 11.4 g (0.05 moles) of antimony trichloride in about 50 cc of refluxing toluene. The solution became dark reddish brown, and the initially formed precipitate redissolved. Reflux continued for two hours, and the solution was then cooled. It contained 3.05 wt% antimony by calculation. Part of the solution was used to treat a catalyst for testing, as outlined below.

후처리

  1. customwas removed
  2. dissolutionthe initially formed precipitate redissolved
  3. temperatureReflux
  4. temperaturethe solution was then cooled
  5. additionto treat a catalyst for testing

출처 및 근거

ORD 기록
ord-b702ff6169cc478faf6d4c525ca8f055
출처 데이터셋
uspto-grants-1981_04
특허 번호
US04264434

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