HCID 20251595, compound → HCID 86739511, compound

HRID 1263184Notes

Reaction equation

HRID 1263184 reaction equation
[CH2:1]([P:3]([C:6]1[CH:11]=[C:10]([O:12][C:13]2[C:18]([Cl:19])=[CH:17][C:16]([C:20]([F:23])([F:22])[F:21])=[CH:15][N:14]=2)[CH:9]=[CH:8][C:7]=1[N+:24]([O-:26])=[O:25])(=[O:5])[OH:4])[CH3:2].[CH3:27][C:28]([CH3:35])([CH3:34])[C:29](=[O:33])[S:30][CH2:31]Cl>>[CH2:1]([P:3]([C:6]1[CH:11]=[C:10]([O:12][C:13]2[C:18]([Cl:19])=[CH:17][C:16]([C:20]([F:23])([F:22])[F:21])=[CH:15][N:14]=2)[CH:9]=[CH:8][C:7]=1[N+:24]([O-:26])=[O:25])(=[O:4])[O:5][CH2:31][S:30][C:29](=[O:33])[C:28]([CH3:35])([CH3:34])[CH3:27])[CH3:2]

Participants

3

Reactant 2

HCID 20251595HCID 20251595, compoundHCID 57210916HCID 57210916, compound

Product 1

HCID 86739511HCID 86739511, compound

Procedure

In the same way, P-ethyl-2-nitro-5-(3-chloro-5-trifluoromethyl-2-pyridyloxy)phenylphosphinic acid is reacted with S-(chloromethyl) 2,2-dimethylpropanothioate to give 2,2-dimethylpropionylthiomethyl P-ethyl-2-nitro-5-(3-chloro-5-trifluoromethyl-2-pyridyloxy)phenylphosphinate.

Sources & evidence

ORD record
ord-6dd4d44b52f342948b2a083c9a0f4d2b
Source dataset
uspto-grants-1984_06
Patent number
US04456465

Reaction notes

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