Hydrochloric Acid → (S)-3,3-Difluoro-5-(hydroxymethyl)pyrrolidin-2-one

HRID 409865Notes

Reaction equation

HRID 409865 reaction equation
[F:1][C:2]1([F:13])[C:11](=[O:12])[N:5]2C(C)(C)[O:7][CH2:8][C@@H:4]2[CH2:3]1.Cl>CO.O1CCOCC1>[F:1][C:2]1([F:13])[CH2:3][C@@H:4]([CH2:8][OH:7])[NH:5][C:11]1=[O:12]

Participants

5

Procedure

To a solution of (S)-6,6-difluoro-3,3-dimethyl-dihydropyrrolo[1,2-c]oxazol-5(1H,3H,6H)-one (1.35 g, 0.706 mmol) in methanol (10 mL) was added HCl in dioxane (2.65 mL, 4N) under ice-water bath and then stirred at RT overnight. The reaction mixture was concentrated. The resulting residue was dissolved in THF (10 mL) and TEA (5 mL) was added. The resulting solution was stirred for 1 h. The reaction mixture was concentrated to give a crude mixture. Purification by flash column chromatography (hexanes/EtOAc) gave (S)-3,3-difluoro-5-(hydroxymethyl)pyrrolidin-2-one (0.80 g 75%). LRMS (M+H+)m/z 152.2.

Workup

  1. concentrationThe reaction mixture was concentrated
  2. dissolutionThe resulting residue was dissolved in THF (10 mL)
  3. additionTEA (5 mL) was added
  4. stirringThe resulting solution was stirred for 1 h
  5. concentrationThe reaction mixture was concentrated
  6. customto give a crude mixture
  7. customPurification by flash column chromatography (hexanes/EtOAc)

Sources & evidence

ORD record
ord-1bc320c6b04b4a81ac57551dc3f2ee09
Source dataset
uspto-grants-2014_06
Patent number
US08759374B2

Reaction notes

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