Hydrochloric Acid → HCID 28804660, compound
Reaction equation
C(OC(=O)[NH:7][C@H:8]([CH2:17][OH:18])[CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([Br:16])[CH:11]=1)(C)(C)C.Cl>CO.O1CCOCC1>[NH2:7][C@@H:8]([CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([Br:16])[CH:11]=1)[CH2:17][OH:18]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of (S)-[2-(3-bromo-phenyl)-1-hydroxymethyl-ethyl]-carbamic acid tert-butyl ester (400 mg, 1.21 mmol) in methanol (30 mL) was added 4 M HCl in dioxane (2 mL, excess). The reaction mixture was stirred at room temperature for 14 h. After concentration in vacuo, the residue was used for the next step without purification. LCMS (M+H)+ m/z 230 (t=0.78 min.)
Workup
- concentrationAfter concentration in vacuo
- customthe residue was used for the next step without purification
- customLCMS (M+H)+ m/z 230 (t=0.78 min.)
Sources & evidence
- ORD record
- ord-c4505e1518444c9489ac35858497daf3
- Source dataset
- uspto-grants-2008_12
- Patent number
- US07470696B2
Reaction notes
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