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Water → HCID 178460683, compound

HRID 2419235
Notes
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Reaction equation

HRID 2419235 reaction equation
[Br:1][C:2]1[CH:8]=[C:7]([Br:9])[CH:6]=[C:5]([Br:10])[C:3]=1[NH2:4].Cl[C:12]([CH:14]([CH3:20])[CH2:15][P:16](Cl)(C)=[O:17])=[O:13].[OH2:21]>>[Br:1][C:2]1[CH:8]=[C:7]([Br:9])[CH:6]=[C:5]([Br:10])[C:3]=1[NH:4][C:12]([CH:14]([CH3:20])[CH2:15][PH:16](=[O:21])[OH:17])=[O:13]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 962WaterHCID 89862,4,6-TribromoanilineHCID 54003998[2-(Chloroformyl-)2-(methyl)ethyl-]methyl phosphinic acid chloride

Product 1

HCID 178460683HCID 178460683, compound

Procedure

330 g (1 mol) of 2,4,6-tribromoaniline was reacted as described in Example 1 with 207 g (1.02 mol) of [2-(chloroformyl-)2-(methyl)ethyl-]methyl phosphinic acid chloride (prepared as described by V. K. Khairullin et al., C.A. 69, 106816 k (1968)). After hydrolysis with 6 liters of water, the resulting [2-(2,4,6-tribromophenylcarbamoyl-) 2-(methyl)ethyl-]methyl phosphinic acid was filtered off and dried at 80° C under vacuum.

Workup

  • filtrationthe resulting [2-(2,4,6-tribromophenylcarbamoyl-) 2-(methyl)ethyl-]methyl phosphinic acid was filtered off
  • customdried at 80° C under vacuum
  • Sources & evidence

    ORD record
    ord-fec1a8bdd3a7421f978ddd31854bd6cd
    Source dataset
    uspto-grants-1978_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04105689

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes