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

HRID 1070207Notes

Reaction equation

HRID 1070207 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-ee8666e30a444fe08ccfca7be0cf89fd
Source dataset
uspto-grants-2001_06
Patent number
US06252078B1

Reaction notes

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