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m-Chloroperbenzoic acid → HCID 13151874, 화합물

HRID 1074979
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반응식

HRID 1074979 반응식
[C:1]([C:3]1[CH:4]=[CH:5][C:6]2[CH:12]=[CH:11][C:10]3[CH:13]=[CH:14][CH:15]=[CH:16][C:9]=3[S:8][C:7]=2[CH:17]=1)#[N:2].ClC1C=CC=C(C(OO)=O)C=1.[OH-:29].[Ca+2].[OH-:31]>C(Cl)Cl>[C:1]([C:3]1[CH:4]=[CH:5][C:6]2[CH:12]=[CH:11][C:10]3[CH:13]=[CH:14][CH:15]=[CH:16][C:9]=3[S:8](=[O:31])(=[O:29])[C:7]=2[CH:17]=1)#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 70297m-Chloroperbenzoic acidHCID 6093208Calcium HydroxideHCID 13490383HCID 13490383, 화합물

생성물 1

HCID 13151874HCID 13151874, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

5.4 G. 3-cyanodibenzo[b,f]thiepin (0.023 mole) are dissolved in 300 cc. methylene chloride and 15.87 g. m-chlorperbenzoic acid (0.092 mole) are added in portions. The resulting solution is stirred at room temperature for one hour, then excess calcium hydroxide is added. The mixture is filtered through celite and the filtrate is stripped to dryness. The yellow solid is triturated in benzene and filtered. One obtains 5.46 g. (89%) of the sulfone, m.p. 229° C.-231° C.

후처리

  1. filtrationThe mixture is filtered through celite
  2. customThe yellow solid is triturated in benzene
  3. filtrationfiltered
  4. customOne obtains 5.46 g

출처 및 근거

ORD 기록
ord-aefe3d021e4a44db9624503aab0104bd
출처 데이터셋
uspto-grants-1983_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04394515

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