Citric Acid → (r)-2-[2-(Tert-butoxy)-2-oxoethyl]-5-cyclohexylpentanoic acid sodium salt
Reaction equation
C1(N)CCCCC1.[C:8]([O:12][C:13](=[O:28])[CH2:14][C@@H:15]([CH2:19][CH2:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[C:16]([OH:18])=[O:17])([CH3:11])([CH3:10])[CH3:9].C(OCC)(=O)C.C(O)(=O)CC(CC(O)=O)(C(O)=O)O.[OH-].[Na+:49]>O>[Na+:49].[C:8]([O:12][C:13](=[O:28])[CH2:14][C@@H:15]([CH2:19][CH2:20][CH2:21][CH:22]1[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27]1)[C:16]([O-:18])=[O:17])([CH3:11])([CH3:9])[CH3:10]Participants
Conditions
- Temperature
- 22.5 °C
Procedure
(R)-2-[2-(tert-Butoxy)-2-oxoethyl]-5-phenylpentanoic acid cyclohexylamine salt (6.8 g, 17 mmol) and ethyl acetate (100 ml) were added to an aqueous solution of citric acid (10%, 100 ml) and the organic phase was separated and washed with water (100 ml). Iso-propyl alcohol (20 ml) and 5% rhodium on alumina (51.69) were added and the mixture was stirred at 20-25° C., under hydrogen (10 atmospheres, 150 p.s.i.) for 48 hours and then filtered through celite. To the filtrate was added a solution of sodium hydroxide (0.67 g, 17 mmol) in water and the mixture was stripped and replaced with acetonitrile by distillation at atmospheric pressure to a volume of 30 ml. The mixture was allowed to cool to 20-25° C. and was stirred for 24 hours. The mixture was cooled to 0° C. and then filtered. The residue was washed with acetonitrile (2×10 ml) and then dried in vacuo at 45° C. for 2 hours to leave the title compound as a colourless solid (3.8 g, 69% yield, 95% pure by NMR).
Workup
- customthe organic phase was separated
- washwashed with water (100 ml)
- additionIso-propyl alcohol (20 ml) and 5% rhodium on alumina (51.69) were added
- filtrationfiltered through celite
- distillationreplaced with acetonitrile by distillation at atmospheric pressure to a volume of 30 ml
- temperatureto cool to 20-25° C.
- stirringwas stirred for 24 hours
- temperatureThe mixture was cooled to 0° C.
- filtrationfiltered
- washThe residue was washed with acetonitrile (2×10 ml)
- customdried in vacuo at 45° C. for 2 hours
Sources & evidence
- ORD record
- ord-9aed7c1d304c4d24aa8baabe08a0396e
- Source dataset
- uspto-grants-2004_06
- Patent number
- US06750363B2
Reaction notes
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