Lithium Hydroxide → HCID 24821992, compound
Reaction equation
[OH-].[Li+].C([N:6]([CH2:15][C@H:16]1[C@H:20]([OH:21])[CH2:19][C@@H:18]([Cl:22])[C@@H:17]1[CH2:23]/[CH:24]=[CH:25]\[CH2:26][CH2:27][CH2:28][C:29]([OH:31])=[O:30])[C:7]1[CH:12]=[C:11]([Cl:13])[CH:10]=[C:9]([Cl:14])[CH:8]=1)(=O)C>C1COCC1>[Cl:22][C@H:18]1[C@H:17]([CH2:23]/[CH:24]=[CH:25]\[CH2:26][CH2:27][CH2:28][C:29]([OH:31])=[O:30])[C@@H:16]([CH2:15][NH:6][C:7]2[CH:8]=[C:9]([Cl:14])[CH:10]=[C:11]([Cl:13])[CH:12]=2)[C@H:20]([OH:21])[CH2:19]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Lithium hydroxide (21 μL of a 1.0 M aqueous solution, 0.021 mmol) was added to a solution of acetate 10 (2 mg, 0.004 mmol) in THF (0.2 mL). After stirring 3 d at room temperature, the reaction mixture was partitioned between aqueous HCl (1.0 N, 2 mL) and EtOAc (2 mL). The phases were separated and the aqueous phase was extracted with EtOAc (2 mL). The combined extracts were dried (MgSO4), filtered and concentrated in vacuo to afford 1 mg (55%) of the title compound (11).
Workup
- customthe reaction mixture was partitioned between aqueous HCl (1.0 N, 2 mL) and EtOAc (2 mL)
- customThe phases were separated
- extractionthe aqueous phase was extracted with EtOAc (2 mL)
- dry with materialThe combined extracts were dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-d45b4d1234744c69b79e996a48aa3e4e
- Source dataset
- uspto-grants-2009_10
- Patent number
- US07605178B2
Reaction notes
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