Methanol → HCID 178501119, compound
Reaction equation
[NH2:1][CH2:2][C@H:3]1[CH2:8][CH2:7][C@H:6]([C:9]([OH:11])=[O:10])[CH2:5][CH2:4]1.S(Cl)([Cl:14])=O.[CH3:16]O>>[ClH:14].[NH2:1][CH2:2][C@H:3]1[CH2:4][CH2:5][C@H:6]([C:9]([O:11][CH3:16])=[O:10])[CH2:7][CH2:8]1Participants
4
Procedure
Trans-4-(aminomethyl)cyclohexanecarboxylic acid (6.29 g) is suspended in methanol (32 ml) and to the suspension is added dropwise thionyl chloride (6 ml) under ice-cooling. The reaction solution is warmed to room temperature, stirred overnight and concentrated under reduced pressure to dryness, which provides methyl trans-4-(aminomethyl)cyclohexanecarboxylate hydrochloride (8.69 g).
Workup
- temperaturecooling
- concentrationconcentrated under reduced pressure to dryness, which
Sources & evidence
- ORD record
- ord-265de67f427e472fad21ee7426d900fb
- Source dataset
- uspto-grants-2009_05
- Patent number
- US07531537B2
Reaction notes
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