Methyl bromoacetate → HCID 54084166, compound

HRID 1284438Notes

Reaction equation

[CH2:1]([P:3]([C:6]1[CH:11]=[C:10]([NH:12][C:13]2[CH:18]=[CH:17][C:16]([C:19]([F:22])([F:21])[F:20])=[CH:15][C:14]=2[N+:23]([O-:25])=[O:24])[CH:9]=[CH:8][C:7]=1[N+:26]([O-:28])=[O:27])(=[O:5])[OH:4])[CH3:2].[CH3:29][O:30][C:31](=[O:34])[CH2:32]Br>>[CH2:1]([P:3]([C:6]1[CH:11]=[C:10]([NH:12][C:13]2[CH:18]=[CH:17][C:16]([C:19]([F:22])([F:20])[F:21])=[CH:15][C:14]=2[N+:23]([O-:25])=[O:24])[CH:9]=[CH:8][C:7]=1[N+:26]([O-:28])=[O:27])(=[O:4])[O:5][CH2:32][C:31]([O:30][CH3:29])=[O:34])[CH3:2]

Participants

Reactant 2

HCID 60984Methyl bromoacetate

HCID 20251605HCID 20251605, compound

Product 1

HCID 54084166HCID 54084166, compound

Procedure

Following the procedure of Example 32, P-ethyl-2-nitro-5-(2-nitro-4-trifluoromethyl-anilino)phenylphosphinic acid is reacted with methylbromoacetate to give methoxycarbonylmethyl P-ethyl-2-nitro-5-(2-nitro-4-trifluoromethylanilino)phenylphosphinate.

Sources & evidence

ORD record: ord-30a20a1099554fa398523b8580c886d9
Source dataset: uspto-grants-1986_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04563310

Reaction notes

Loading…