tert-Butyl hydroperoxide → ((2R,3R)-3-(4-chloro-3-fluorophenyl)oxiran-2-yl)methanol

HRID 2365804Notes

Reaction equation

HRID 2365804 reaction equation
C([C@H]([C@@H](C(OC(C)C)=O)O)O)(OC(C)C)=[O:2].C(OO)(C)(C)C.[Cl:23][C:24]1[CH:29]=[CH:28][C:27](/[CH:30]=[CH:31]/[CH2:32][OH:33])=[CH:26][C:25]=1[F:34]>ClCCl.CC(C)[O-].[Ti+4].CC(C)[O-].CC(C)[O-].CC(C)[O-]>[Cl:23][C:24]1[CH:29]=[CH:28][C:27]([C@H:30]2[O:2][C@@H:31]2[CH2:32][OH:33])=[CH:26][C:25]=1[F:34]

Participants

6

Conditions

Temperature
-20 °C

Procedure

Diisopropyl D-tartrate (1.690 mL, 8.038 mmol) was dissolved in dichloromethane (500 mL) and cooled to −20° C. Activated powdered 4 Å molecular sieves (3 g), titanium(IV) isopropoxide (1.570 mL, 5.359 mmol) and tert-butyl hydroperoxide (19.49 mL, 107.2 mmol; in decane) were added sequentially, and the mixture was agitated for 1 hour at −20° C. (E)-3-(4-Chloro-3-fluorophenyl)prop-2-en-1-ol (10.0 g, 53.59 mmol) was dissolved in dichloromethane (25 mL) and treated with 4 Å molecular sieves (1.0 g) for 1 hour. This mixture was added to the initial mixture over 20 minutes and agitation was continued for another 3 hours at −20° C. The reaction was then quenched by addition of a mixture of a saturated NaCl solution (3 mL) and 50% w/v NaOH (3 mL). Ether was added (100 mL), and the mixture was allowed to warm up to 10° C. After agitating for 10 minutes at this temperature, MsSO4 (5 g) and Celite® (2 g) were added, and the mixture was agitated for an additional 15 minutes. The mixture was then allowed to settle and filtered through a pad of Celite®, washing with ether. Solvents were then evaporated, and resulting solid was triturated with hexane to give ((2R,3R)-3-(4-chloro-3-fluorophenyl)oxiran-2-yl)methanol (10.55 g, 52.07 mmol, 97.17% yield) as a solid.

Workup

  1. additionwere added sequentially
  2. additiontreated with 4 Å molecular sieves (1.0 g) for 1 hour
  3. customThe reaction was then quenched by addition of a mixture of a saturated NaCl solution (3 mL) and 50%
  4. additionEther was added (100 mL)
  5. temperatureto warm up to 10° C
  6. additionwere added
  7. stirringthe mixture was agitated for an additional 15 minutes
  8. filtrationfiltered through a pad of Celite®
  9. washwashing with ether
  10. customSolvents were then evaporated
  11. customresulting solid
  12. customwas triturated with hexane

Sources & evidence

ORD record
ord-3670d1812a9e4ff1a4c83dfe9cffe207
Source dataset
uspto-grants-2014_04
Patent number
US08697715B2

Reaction notes

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