Hydrochloric Acid → HCID 12761781, compound
Reaction equation
[ClH:1].[O:2]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[O:5][CH2:4][CH:3]1[CH2:12][C:13]1[NH:14][C:15]2[CH:21]=[CH:20][CH:19]=[CH:18][C:16]=2[N:17]=1.C(OCC)C>CO>[ClH:1].[O:2]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[O:5][CH2:4][CH:3]1[CH2:12][C:13]1[NH:17][C:16]2[CH:18]=[CH:19][CH:20]=[CH:21][C:15]=2[N:14]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Excess 3% hydrogen chloride in methanol is added to a solution of 1.0 g. 2-(1,4-benzodioxan-2-ylmethyl)-benzimidazole in 20 ml methanol. Diethyl ether is added until precipitation is complete. The product is filtered, washed with ether, air dried and recrystallized from methanol/acetone to yield 2-(1,4-benzodioxan-2-ylmethyl)benzimidazole hydrochloride, m.p. 221°-224° C.(d).
Workup
- filtrationThe product is filtered
- washwashed with ether, air
- customdried
- customrecrystallized from methanol/acetone
Sources & evidence
- ORD record
- ord-8b575e3ad9084972b5dc20d96bdc3e6f
- Source dataset
- uspto-grants-1981_11
- Patent number
- US04301171
Reaction notes
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