Pentane → 2-(2-tert-Butylphenyl)-4,4-dimethyl-4,5-dihydro-1,3-oxazole

HRID 1938941Notes

Reaction equation

HRID 1938941 reaction equation
[Li][C:2]([CH3:5])([CH3:4])[CH3:3].CCCCC.F[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[C:18]1[O:19][CH2:20][C:21]([CH3:24])([CH3:23])[N:22]=1>C1COCC1>[C:2]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[C:18]1[O:19][CH2:20][C:21]([CH3:24])([CH3:23])[N:22]=1)([CH3:5])([CH3:4])[CH3:3]

Participants

5

Procedure

A 1.7M solution of t-BuLi in pentane (161 mL, 274 mmol) was added dropwise to a solution of 2-(2-fluorophenyl)-4,4-dimethyl-2-oxazoline [cf. Meyers A. I. and Williams B. E., Tetrahedron Letters, 223-226(1978)] (48.0 g., 249 mmol) in THF (320 mL), maintaining the reaction temperature between -45° and -40° C. with a dry-ice/acetone cooling bath. The resulting reaction mixture was maintained at ≤-40° C. with a dry-ice/acetonitrile bath, and monitored to completion by GLC over 20 min. This mixture was poured onto ice and extracted three times with ether. These extracts were combined, dried (MgSO4), concentrated and distilled under vacuum to afford 56.87 g of 2-(2-tert-butylphenyl)-4,4-dimethyl-2-oxazoline, a 93% yield.

Workup

  1. temperaturemaintaining the reaction temperature between -45° and -40° C. with a dry-ice/acetone cooling bath
  2. customThe resulting reaction mixture
  3. temperaturewas maintained at ≤-40° C. with a dry-ice/acetonitrile bath
  4. additionThis mixture was poured onto ice
  5. extractionextracted three times with ether
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated
  8. distillationdistilled under vacuum

Sources & evidence

ORD record
ord-ea594dafc67a4271aa6867e6df4c0440
Source dataset
uspto-grants-1997_12
Patent number
US05693667

Reaction notes

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