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Hydrogen Bromide → [2-(2-Thienyl)ethylamino](2-chlorophenyl)acetamide hydrobromide

HRID 1384476
Notes
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Reaction equation

HRID 1384476 reaction equation
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][CH2:7][NH:8][CH:9]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[Cl:19])[C:10]([NH2:12])=[O:11].[BrH:20]>CC(C)=O>[BrH:20].[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][CH2:7][NH:8][CH:9]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[Cl:19])[C:10]([NH2:12])=[O:11]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 260Hydrogen BromideHCID 9882604[2-(2-Thienyl)ethylamino](2-chlorophenyl)acetamide

Product 1

HCID 21187054[2-(2-Thienyl)ethylamino](2-chlorophenyl)acetamide hydrobromide

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

14.7 g (0.05 mol) of [2-(2-thienyl)ethylamino](2-chlorophenyl)acetamide, prepared as described in Example 7, is dissolve din 150 ml of acetone. To the solution 4 ml of 60% aqueous hydrogen bromide solution is added and the precipitated white crystals are filtered off, washed with acetone and dried.

Workup

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
  1. dissolutionis dissolve
  2. filtrationthe precipitated white crystals are filtered off
  3. washwashed with acetone
  4. customdried

Sources & evidence

ORD record
ord-3aa938a98c254de18ce0bedfd69008d4
Source dataset
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06258961B1

Reaction notes

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