Tetrahydrofuran → tert-butyl (3R)-4-hydroxy-3-methylbutyrate
Reaction equation
[CH3:1][C@@H:2]([C:11]([O-])=[O:12])[CH2:3][C:4]([O:6][C:7]([CH3:10])([CH3:9])[CH3:8])=[O:5].C1COCC1>CO>[OH:12][CH2:11][C@H:2]([CH3:1])[CH2:3][C:4]([O:6][C:7]([CH3:10])([CH3:9])[CH3:8])=[O:5]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -10 °C
Procedure
Borane-dimethyl sulphide complex (10M, 10.3 ml) was added over 15 min to a stirred mixture of 1-tert-butyl (3R)-3-methylsuccinate (12.9 g) and THF (200 ml) which had been cooled to -10° C. and placed under an atmosphere of argon. The mixture was stirred at -10° C. for 30 min. The mixture was allowed to warm to room temperature and stirred for 1 hour. The mixture was recooled to 5 C. and methanol (50 ml) was added portionwise. The mixture was allowed to warm to room temperature and stirred for 30 min. The mixture was evaporated and the residue partitioned between dichloromethane (100 ml) and water (100 ml). The organic phase was filtered through phase separating paper and evaporated to give tert-butyl (3R)-4-hydroxy-3-methylbutyrate as an oil (11 g); NMR (CDCl3) δ 3.55(2H,m), 2.1-2.4(3H,m), 1.46(9H,s), 0.98(3H,d).
Workup
- temperatureto warm to room temperature
- stirringstirred for 1 hour
- temperatureto warm to room temperature
- stirringstirred for 30 min
- customThe mixture was evaporated
- customthe residue partitioned between dichloromethane (100 ml) and water (100 ml)
- filtrationThe organic phase was filtered through phase
- customseparating paper
- customevaporated
Sources & evidence
- ORD record
- ord-5987c1842c0d4a70aaaba7918e334856
- Source dataset
- uspto-grants-1998_05
- Patent number
- US05750754
Reaction notes
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