Hydrochloric Acid → HCID 12033612, compound
Reaction equation
[OH:1][C@@H:2]1[CH2:6][CH2:5][C@H:4]([C:7]([O-:9])=[O:8])[C@H:3]1[C:10]1[CH:15]=[CH:14][C:13]([F:16])=[CH:12][CH:11]=1.C[C@H]([NH3+])C1C=CC=CC=1.Cl.CCO>O>[OH:1][C@@H:2]1[CH2:6][CH2:5][C@H:4]([C:7]([OH:9])=[O:8])[C@H:3]1[C:10]1[CH:15]=[CH:14][C:13]([F:16])=[CH:12][CH:11]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The salt from Step B was dissolved in water and acidified with 2N HCl and was extracted with 3 portions of EtOAc. The organic layers were washed with a portion of brine, combined, dried over sodium sulfate and evaporated to give a white solid. [α]D (EtOH)=+21.6 (c=2.55).
Workup
- extractionwas extracted with 3 portions of EtOAc
- washThe organic layers were washed with a portion of brine
- dry with materialdried over sodium sulfate
- customevaporated
- customto give a white solid
Sources & evidence
- ORD record
- ord-2b769177d20148058ac84cc9136247be
- Source dataset
- uspto-grants-1999_03
- Patent number
- US05877191
Reaction notes
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