Lithium Hydroxide → HCID 53816519, compound
Reaction equation
C[O:2][C:3](=[O:19])[CH2:4][C@@:5]([OH:18])([CH2:9][CH2:10][C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=1)[CH:6]([CH3:8])[CH3:7].[OH-].[Li+]>CO.O>[OH:18][C@:5]([CH2:9][CH2:10][C:11]1[CH:12]=[CH:13][C:14]([OH:17])=[CH:15][CH:16]=1)([CH:6]([CH3:7])[CH3:8])[CH2:4][C:3]([OH:19])=[O:2]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
The title compound was prepared by dissolving (S)-3-hydroxy-3-[2-(4-hydroxy-phenyl)-ethyl]-4-methyl-pentanoic acid methyl ester (0.57 g, 2.15 mmol) from Example TTTT in MeOH (30 mL). Lithium hydroxide (0.18 g, 4.29 mmol) in water (10 mL) was added and the reaction heated to reflux for 1 hour, cooled and pumped to dryness under vacuum. The product was partitioned between water and Et2O. The aqueous layer was decanted, acidified with 1N HCl and extracted with Et2O. The solution was dried (MgSO4) and concentrated to give the title compound (m.p. 137°-140° C.).
Workup
- customThe title compound was prepared
- temperaturethe reaction heated
- temperatureto reflux for 1 hour
- temperaturecooled
- customThe product was partitioned between water and Et2O
- customThe aqueous layer was decanted
- extractionextracted with Et2O
- dry with materialThe solution was dried (MgSO4)
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-08779c52040c485a8d80a41b4285eacc
- Source dataset
- uspto-grants-1998_11
- Patent number
- US05834506
Reaction notes
Loading…