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m-Chloroperbenzoic acid → 2-(2,6-Dimethylphenyl)sulfinyl-5-methyl-1,3,4-oxadiazole

HRID 1379090
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HRID 1379090 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[S:9][C:10]1[O:11][C:12]([CH3:15])=[N:13][N:14]=1.C1C=C(Cl)C=C(C(OO)=[O:24])C=1>C(Cl)Cl>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[S:9]([C:10]1[O:11][C:12]([CH3:15])=[N:13][N:14]=1)=[O:24]
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참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 229096302-(2,6-Dimethylphenyl)thio-5-methyl-1,3,4-oxadiazole

생성물 1

HCID 229096442-(2,6-Dimethylphenyl)sulfinyl-5-methyl-1,3,4-oxadiazole수율 33.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To an ice-cooled solution of 2-(2,6-dimethylphenyl)thio-5-methyl-1,3,4-oxadiazole (0.350 g, 0.0016 mol) in CH2Cl2 (10 ml) was added dropwise m-CPBA (0.530 g, 0.002 mol, 65% pure) in CH2Cl2 (5 ml). The ice bath was removed and the reaction mixture was stirred at rt for 2 h and treated with sat. aq. Na2S2O3 (2.5 ml) solution and sat. aq. Na2CO3 (10 ml). The organic layer was separated and then the aqueous layer was extracted with CH2Cl2 (2×25 ml), dried (MgSO4) and the solvent evaporated in vacuo. Chromatography on silica gel using ethyl acetate/hexanes (1/1) as the eluant gave 2-(2,6-dimethylphenyl)sulfinyl-5-methyl-1,3,4-oxadiazole (78) (0.125 g, 23%) as a white solid; mp 79°-80° C.

후처리

  1. customThe ice bath was removed
  2. additiontreated with sat. aq. Na2S2O3 (2.5 ml) solution and sat. aq. Na2CO3 (10 ml)
  3. customThe organic layer was separated
  4. extractionthe aqueous layer was extracted with CH2Cl2 (2×25 ml)
  5. dry with materialdried (MgSO4)
  6. customthe solvent evaporated in vacuo

출처 및 근거

ORD 기록
ord-0988530654dc47f4bdb1cc298d3775ac
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05670526

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