N-bromobutanimide → Silver bromide

HRID 1390800Notes

Reaction equation

HRID 1390800 reaction equation
[C:1]([O-:24])(=[O:23])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22].[Ag+:25].[Br:26]N1C(=O)CCC1=O>CC(C)=O>[Ag:25][Br:26].[C:1]([O-:24])(=[O:23])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22].[Ag+:25]

Participants

5

Reactant 2

HCID 67184N-bromobutanimide2×HCID 164971Silver behenate

Product 2

HCID 66199Silver bromideHCID 164971Silver behenate

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent2×

Procedure

Next, while the thus-obtained polymer dispersion of silver behenate was maintained at a temperature of 50° C. and stirred at 500 r.p.m., an acetone solution of N-bromosuccinimide prepared at 25° C. (0.7 g of N-bromosuccinimide and 50 ml of acetone) was added thereto. The resulting mixture was further stirred for 60 minutes. Thus, a polymer dispersion of silver bromide and silver behenate was obtained.

Workup

  1. additionwas added
  2. stirringThe resulting mixture was further stirred for 60 minutes

Sources & evidence

ORD record
ord-c3e13256993645078a71fe8258267d2b
Source dataset
uspto-grants-1979_02
Patent number
US04140532

Reaction notes

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