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m-Chloroperbenzoic acid → HCID 20232107, 화합물

HRID 2290337
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HRID 2290337 반응식
ClC1C=CC=C(C(OO)=[O:9])C=1.[CH3:12][C:13]1[N:14]=[C:15]([S:25][CH3:26])[N:16]=[N:17][C:18]=1[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>C(Cl)(Cl)Cl>[CH3:12][C:13]1[N:14]=[C:15]([S:25]([CH3:26])=[O:9])[N:16]=[N:17][C:18]=1[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 155863425-Methyl-3-methylthio-6-phenyl-1,2,4-triazine

생성물 1

HCID 20232107HCID 20232107, 화합물수율 88.5%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

m-Chloroperbenzoic acid (20 g) was added to a stirred solution of 5-methyl-3-methylthio-6-phenyl-1,2,4-triazine (20 g) in chloroform (600 ml) under ice cooling, and the mixture was stirred for 30 minutes at room temperature. The reaction mixture was washed with a saturated aqueous solution of sodium bicarbonate, dried over sodium sulfate, and then concentrated. The resulting residue was crystallized with diethyl ether, and the crystals were collected by filtration, washed with diethyl ether and dried to give 5-methyl-3-methylsulfinyl-6-phenyl-1,2,4-triazine (19.0 g).

후처리

  1. washThe reaction mixture was washed with a saturated aqueous solution of sodium bicarbonate
  2. dry with materialdried over sodium sulfate
  3. concentrationconcentrated
  4. customThe resulting residue was crystallized with diethyl ether
  5. filtrationthe crystals were collected by filtration
  6. washwashed with diethyl ether
  7. customdried

출처 및 근거

ORD 기록
ord-a4b4184592cf4e1da36ce71f8b34d588
출처 데이터셋
uspto-grants-1986_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04616014

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