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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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m-Chloroperbenzoic acid → 2-(2,4-Dichlorophenylmethylsulfinyl)pyridine N-oxide

HRID 329145
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반응식

HRID 329145 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH2:9][S:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][N+:12]=1[O-:17].C1C=C(Cl)C=C(C(OO)=[O:26])C=1>C(Cl)(Cl)Cl>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH2:9][S:10]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][N+:12]=1[O-:17])=[O:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 470955022-(2,4-dichlorophenylmethylthio)pyridine N-oxide

생성물 1

HCID 544932542-(2,4-Dichlorophenylmethylsulfinyl)pyridine N-oxide

시약·촉매·용매 1

HCID 6212Chloroform용매2회

실험 절차

A well stirred solution of 5.8 gms (0.02 mole) of 2-(2,4-dichlorophenylmethylthio)pyridine N-oxide in 50 ml of chloroform is treated at 0° - 10° with 4 gms (0.02 mole) MCPBA (85%) in 50 ml of chloroform. The mixture is allowed to rise to ambient and held for 16 hours. The reaction mixture is washed with saturated sodium bicarbonate, dried and evaporated to 5.5 gms (89% theory) of product. Melting point 138° - 141° C. Structure confirmed by IR and NMR. (IR N-O 1240 cm-1, SO 1050 cm-1)

후처리

  1. washThe reaction mixture is washed with saturated sodium bicarbonate
  2. customdried
  3. customevaporated to 5.5 gms (89% theory) of product

출처 및 근거

ORD 기록
ord-a3488cbde498442392d03e062a4c02ed
출처 데이터셋
uspto-grants-1977_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04019893

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