Phosphate → 2-(3,4-Difluorophenyl)-2-methyloxirane

HRID 1275211노트

반응식

HRID 1275211 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:10])=[CH2:9])=[CH:4][C:3]=1[F:11].P([O-])([O-])([O-])=[O:13].ClC1C=C(C=CC=1)C(OO)=O>C(Cl)Cl>[F:11][C:3]1[CH:4]=[C:5]([C:8]2([CH3:10])[CH2:9][O:13]2)[CH:6]=[CH:7][C:2]=1[F:1]

참가 물질

5

반응물 3

HCID 1061PhosphateHCID 70297m-Chloroperbenzoic acidHCID 155252121,2-Difluoro-4-(prop-1-en-2-yl)benzene

생성물 1

HCID 229935082-(3,4-Difluorophenyl)-2-methyloxirane

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a biphasic solution of 1,2-difluoro-4-isopropenyl-benzene (0.81 g, 5.1 mmol) in CH2Cl2 (50 mL) and 50 mL of phosphate buffer (made by dissolving 0.3 g of NaHPO4 and 0.35 g of NaH2PO4 in 50 mL water, pH=8) at 0° C., was added a solution of 3-chloroperoxybenzoic acid (approx. 75% solid, 3.32 g, 10.2 mmol) via a dropping funnel fitted with a cotton plug dropwise in two batches. The solution was stirred at room temperature overnight. It was extracted with CH2Cl2, washed with sat. Na2S2O4 solution followed by water. The organic layer was finally washed with sat. NaHCO3, separated, dried over Na2SO4, filtered and solvent was removed in vacuo. 2-(3,4-Difluorophenyl)-2-methyl-oxirane was obtained as a pale yellow oil (0.65 g, 74% yield). It was used in the next step without purification.

후처리

  1. customfitted with a cotton plug dropwise in two batches
  2. extractionIt was extracted with CH2Cl2
  3. washwashed with sat. Na2S2O4 solution
  4. washThe organic layer was finally washed with sat. NaHCO3
  5. customseparated
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. customsolvent was removed in vacuo

출처 및 근거

ORD 기록
ord-854da8be63b4464a8b5507abbf4f34ae
출처 데이터셋
uspto-grants-2000_12
특허 번호
US06159990

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