Methanol → Methyl 1-aminocyclobutane-1-carboxylate hydrochloride
Reaction equation
Cl.[NH2:2][C:3]1([C:7]([OH:9])=[O:8])[CH2:6][CH2:5][CH2:4]1.S(Cl)([Cl:12])=O.[CH3:14]O>>[ClH:12].[CH3:14][O:8][C:7]([C:3]1([NH2:2])[CH2:6][CH2:5][CH2:4]1)=[O:9]Participants
4
Procedure
1-aminocyclobutanecarboxylic acid hydrochloride (5.2 g, 34.5 mmol) and methanol (120 ml) were charged. An ice bath was set and thionyl chloride (3.7 ml, 51.7 mmol) was slowly added thereto. Then, the ice bath was removed, and the mixture was stirred at room temperature for 3 hours. The resultant product was vacuum-distilled to remove a solvent, and dried in a 60° C. oven so as to obtain methyl-1-aminocyclobutanecarboxylate hydrochloride (5.62 g, 37.1 mmol, 98%).
Workup
- customAn ice bath was set
- customThen, the ice bath was removed
- distillationThe resultant product was vacuum-distilled
- customto remove a solvent
- customdried in a 60° C. oven so as
Sources & evidence
- ORD record
- ord-125da39c2b5e43409109e0b235295156
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09073830B2
Reaction notes
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