Sodium Hydroxide → 4-(Morpholin-3-on-4-yl)-3-trifluoromethyl-benzoic acid

HRID 551167노트

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HRID 551167 반응식
[N:1]1([C:7]2[CH:15]=[CH:14][C:10]([C:11]([OH:13])=[O:12])=[CH:9][C:8]=2[C:16]([F:19])([F:18])[F:17])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[OH-].[Na+].[Mn]([O-])(=O)(=O)=[O:23].[K+].S([O-])([O-])(=O)=S.[Na+].[Na+]>O>[N:1]1([C:7]2[CH:15]=[CH:14][C:10]([C:11]([OH:13])=[O:12])=[CH:9][C:8]=2[C:16]([F:17])([F:19])[F:18])[CH2:6][CH2:5][O:4][CH2:3][C:2]1=[O:23]

참가 물질

6

반응물 4

HCID 14798Sodium HydroxideHCID 24477Sodium ThiosulfateHCID 516875Potassium PermanganateHCID 594957964-Morpholin-4-yl-3-(trifluoromethyl)benzoic acid

생성물 1

HCID 670485144-(Morpholin-3-on-4-yl)-3-trifluoromethyl-benzoic acid

시약·촉매·용매 1

HCID 962Water용매

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온도
45 °C

실험 절차

1.00 g (3.63 mmol) 4-(morpholin-4-yl)-3-trifluoromethyl-benzoic acid (prepared by synthesis sequence analogously to Example 13a and 13b) is suspended in 40 ml of water and 150 mg (3.75 mmol) sodium hydroxide are added. Then 1.73 g (10.92 mmol) potassium permanganate are added and the mixture is stirred for 1.5 hours at 45° C. Then the reaction mixture is cooled in the ice bath and sodium thiosulphate is added until total decolorisation is obtained. After extraction 3 times with ethyl acetate the combined organic phases are dried over sodium sulphate evaporated down i. vac. After application of the residue to silica gel it is purified by chromatography on silica gel (eluant: dichloromethane/methanol 95:5).

후처리

  1. additionis added until total decolorisation
  2. customis obtained
  3. extractionAfter extraction 3 times with ethyl acetate the combined organic phases
  4. dry with materialare dried over sodium sulphate
  5. customevaporated down i
  6. customAfter application of the residue to silica gel it is purified by chromatography on silica gel (eluant: dichloromethane/methanol 95:5)

출처 및 근거

ORD 기록
ord-a35ae71513d740d4aa0e80fde50e889b
출처 데이터셋
uspto-grants-2011_05
특허 번호
US07947700B2

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