Hydrogen chloride-ethyl acetate → HCID 67304349, compound
Reaction equation
C(OC([N:8]([CH2:16][C:17]1[CH:18]=[C:19]([CH:23]=[CH:24][C:25]=1[F:26])[C:20]([OH:22])=[O:21])C(OC(C)(C)C)=O)=O)(C)(C)C.[ClH:27].[C:28](OCC)(=O)[CH3:29]>C(OCC)(=O)C>[ClH:27].[NH2:8][CH2:16][C:17]1[CH:18]=[C:19]([CH:23]=[CH:24][C:25]=1[F:26])[C:20]([O:22][CH2:28][CH3:29])=[O:21]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2.59 g of 3-{[bis(tert-butoxycarbonyl)amino]methyl}-4-fluorobenzoic acid was dissolved in 10.0 mL of ethyl acetate, and 10.0 mL of a 4 M hydrogen chloride/ethyl acetate solution was added thereto, followed by stirring at room temperature for 4 hours. The reaction liquid was concentrated under reduced pressure, and the obtained residue was crystallized by addition of ethyl acetate and hexane to obtain 2.59 g of ethyl 3-(aminomethyl)-4-fluorobenzoate hydrochloride.
Workup
- customThe reaction liquid
- concentrationwas concentrated under reduced pressure
- customthe obtained residue was crystallized by addition of ethyl acetate and hexane
Sources & evidence
- ORD record
- ord-abec6d6fe02147ae9ab15354dfa68f36
- Source dataset
- uspto-grants-2011_07
- Patent number
- US07973078B2
Reaction notes
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