Tetrahydrofuran → tert-butyl (3R)-4-hydroxy-3-methylbutyrate

HRID 1290555Notes

Reaction equation

HRID 1290555 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

4

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

  1. temperatureto warm to room temperature
  2. stirringstirred for 1 hour
  3. temperatureto warm to room temperature
  4. stirringstirred for 30 min
  5. customThe mixture was evaporated
  6. customthe residue partitioned between dichloromethane (100 ml) and water (100 ml)
  7. filtrationThe organic phase was filtered through phase
  8. customseparating paper
  9. customevaporated

Sources & evidence

ORD record
ord-5987c1842c0d4a70aaaba7918e334856
Source dataset
uspto-grants-1998_05
Patent number
US05750754

Reaction notes

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