Ammonia → 4-Methylimidazol-5-ylmethanolhydrochloride
Reaction equation
N.[Ca].C([O:5][C:6]([C:8]1[N:9]=[CH:10][NH:11][C:12]=1[CH3:13])=O)C.[Cl-:14].[NH4+]>C(O)(C)C.CO.C(O)(C)(C)C>[ClH:14].[OH:5][CH2:6][C:8]1[N:9]=[CH:10][NH:11][C:12]=1[CH3:13]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
A 2 liter flask, fitted with an overhead stirrer and a nitrogen inlet, was charged with 700 ml. of anhydrous ammonia. Calcium (29.0 g., 0.723 m.) was added carefully in portions. t-Butanol (25 ml., 0.266 m.) was added in one portion and 5-methyl-4-imidazolecarboxylic acid ethyl ester (50 g., 0.32 m.) was added in portions over 30 minutes. The blue solution was stirred for 40 minutes and methanol (120 ml.) added dropwise. Ammonium chloride (80.0 g., 1.48 m.) and isopropanol (800 ml.) were added and the ammonia removed. Hydrogen chloride gas was added (pH about 1) and the solids filtered off. The filtrate was concentrated to 100 ml. and acetone (500 ml.) was added. The product was collected and dried to give 4-hydroxymethyl-5-methylimidazole hydrochloride (23.0 g. of 65% pure material; yield 30%).
Workup
- customA 2 liter flask, fitted with an overhead stirrer and a nitrogen inlet
- additionwas charged with 700 ml
- additionwas added in portions over 30 minutes
- customthe ammonia removed
- additionHydrogen chloride gas was added (pH about 1)
- filtrationthe solids filtered off
- concentrationThe filtrate was concentrated to 100 ml
- additionand acetone (500 ml.) was added
- customThe product was collected
- customdried
Sources & evidence
- ORD record
- ord-5d4b2a281c11476cb528d11b31182358
- Source dataset
- uspto-grants-1977_12
- Patent number
- US04063023
Reaction notes
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