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Acetic Acid → 4,5,6,7-Tetrahydro-2-benzimidazolone

HRID 1585212
Notes
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Reaction equation

HRID 1585212 reaction equation
Br[CH:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C:3]1=O.[NH2:9][C:10]([NH2:12])=[O:11].C([O-])(=O)C.[NH4+].C(O)(=O)C>O>[N:9]1[C:10](=[O:11])[N:12]=[C:2]2[CH2:7][CH2:6][CH2:5][CH2:4][C:3]=12
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 1176UreaHCID 517165Ammonium AcetateHCID 117897582-Bromocyclohexanone

Product 1

HCID 232922894,5,6,7-Tetrahydro-2-benzimidazolone

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

A mixture of 2-bromocyclohexanone (6.23 g, 0.035 mol) and urea (2.1 g, 0.035 mol) is refluxed in a solution of ammonium acetate (10 g), acetic acid (15 mL) and water (5 mL) for 4 h. Upon cooling slowly to room temp, white crystals form in the reaction vessel. The solid is collected by suction filtration, washed thoroughly with water and ether, and dried in vacuo to afford 4,5,6,7-tetrahydro-2-benzimidazolone (Compound 7). ##STR47##

Workup

  1. filtrationThe solid is collected by suction filtration
  2. washwashed thoroughly with water and ether
  3. customdried in vacuo

Sources & evidence

ORD record
ord-4cabce1a5c9240b0a2d3e8fd7fe41fce
Source dataset
uspto-grants-1999_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05936095

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes