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Phosphorus oxychloride → 145980-57-0

HRID 1379299
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인쇄 미리보기

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HRID 1379299 반응식
[F:1][C:2]([F:15])([F:14])[C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([CH3:9])[C:4]=1[S:10]([O-])(=[O:12])=[O:11].[Na+].P(Cl)(Cl)([Cl:19])=O>CCOCC>[F:1][C:2]([F:15])([F:14])[C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([CH3:9])[C:4]=1[S:10]([Cl:19])(=[O:12])=[O:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 23708595HCID 23708595, 화합물

생성물 1

HCID 11032589145980-57-0

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

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온도
0 °C

실험 절차

A mixture of 290 g of sodium 2-trifluoromethyl-6-methylbenzenesulfonate and 500 mL of phosphorous oxychloride was heated to reflux for 5 hours. The mixture was then cooled to 0° C. and poured into a large flask containing 2000 g of ice and 2 L of ether. After stirring for 30 minutes, the phases were separated and the organic phase washed with cold water, cold saturated aqueous sodium carbonate, and then brine. The solvent was removed in vacuo to yield 2-trifluoromethyl-6-methylbenzenesulfonyl chloride as a brown oil.

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후처리

  1. temperaturewas heated
  2. temperatureto reflux for 5 hours
  3. additionpoured into a large flask
  4. customthe phases were separated
  5. washthe organic phase washed with cold water, cold saturated aqueous sodium carbonate
  6. customThe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-644cf988274e437c98fd00bdce79223c
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05670691

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