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m-Chloroperbenzoic acid → 2-(2,4-Dichlorophenylmethylsulfinyl)pyridine N-oxide

HRID 1112070
Notes
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Reaction equation

HRID 1112070 reaction equation
[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]
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 2

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 6212ChloroformSolvent2×

Procedure

The procedure employed is identical to that of Example 68 using 5.8 gm (0.02 mol) 2-(2,4-Dichlorophenylmethylthio)pyridine N-oxide in 50 ml of chloroform and 4 gm (0.02 mol) MCPBA in 100 ml of chloroform.

Sources & evidence

ORD record
ord-3e419111ba814ca7a1db8265692c2cbd
Source dataset
uspto-grants-1978_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04120692

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes