Water → di-O-isopropyl P-[[(2-trifluoromethyl-6-methylphenyl)sulfonyloxy]methyl]phosphonate

HRID 1379300노트

반응식

HRID 1379300 반응식
[OH-].[Na+].O.[OH:4][CH2:5][P:6](=[O:15])([O:11][CH:12]([CH3:14])[CH3:13])[O:7][CH:8]([CH3:10])[CH3:9].[F:16][C:17]([F:30])([F:29])[C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([CH3:24])[C:19]=1[S:25](Cl)(=[O:27])=[O:26]>[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1.C1(C)C=CC=CC=1>[F:30][C:17]([F:16])([F:29])[C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([CH3:24])[C:19]=1[S:25]([O:4][CH2:5][P:6](=[O:15])([O:7][CH:8]([CH3:10])[CH3:9])[O:11][CH:12]([CH3:14])[CH3:13])(=[O:27])=[O:26]

참가 물질

7

실험 절차

A mixture of 100 mL of toluene, 11.6 g of 50% aqueous sodium hydroxide solution, and 10 mL of water was cooled in an ice bath and treated with 1.3 g of benzyltriethylammonium chloride and 12.0 g of diisopropyl P-(hydroxymethyl)phosphonate (prepared as in U.S. Pat. No. 5,272,128) and stirred vigorously. To this was added a solution of 15 g of the compound of Example 16 (2-trifluoromethyl-6-methylbenzenesulfonyl chloride) in 10 mL of toluene. The cooling bath was removed and the mixture stirred for one hour, then the layers were separated. The organic phase was washed with water (2×100 mL) and brine, then dried through calcium sulfate to yield 23 g of di-O-isopropyl P-[[(2-trifluoromethyl-6-methylphenyl)sulfonyloxy]methyl]phosphonate as a brown oil.

후처리

  1. temperaturewas cooled in an ice bath
  2. customprepared as in U.S
  3. customThe cooling bath was removed
  4. stirringthe mixture stirred for one hour
  5. customthe layers were separated
  6. washThe organic phase was washed with water (2×100 mL) and brine
  7. dry with materialdried through calcium sulfate

출처 및 근거

ORD 기록
ord-140f843c4fa241a59177c71f7bba39ac
출처 데이터셋
uspto-grants-1997_09
특허 번호
US05670691

반응 노트

불러오는 중…