Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 59066510 | HCID 59066510 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69890998 | HCID 69890998 | 61% |
Reaction Steps
To a −78° C. solution of (4S)-3-{[(2S,3S)-3-(2-fluorophenyl)-1-methyl-5-oxopyrrolidin-2-yl]carbonyl}-4-benzyl-1,3-oxazolidin-2-one (1.0 g, 2.5 mmol) in anhyd. THF (30 mL) was added a solution of LiAlH4 (1M in THF, 2.5 mL, 2.5 mmol, 1 equiv). After 2 h a solution of LiAlH4 (1M in THF, 0.5 mL, 0.5 mmol, 0.2 equiv) was added and after 30 min the reaction was treated with a saturated NH4Cl solution (10 mL). The resulting mixture was allowed to warm to room temperature and filtered. The filtrate was concentrated under reduced pressure and purified by flash chromatography (50 g silica gel, gradient from 0% to 10% MeOH/EtOAc) to afford (4S,5S)-4-(2-fluorophenyl)-5-(hydroxymethyl)-1-methylpyrrolidin-2-one (340 mg, 61%) as a white solid: TLC (5% MeOH/EtOAc) Rf 0.40; 1H NMR (CDCl3) δ 2.41 (dd, J=8.4, 15.8 Hz, 1H), 2.94 (s, 3H), 3.03 (dd, J=11.6, 16.0 Hz, 1H), 3.21 (dd, J=2.2, 12.5 Hz, 1H), 3.53 (br s, 1H), 3.67 (dd, J=2.2, 12.5 Hz, 1H), 3.81-3.85 (m, 1H), 3.94-4.03 (m, 1H), 7.04 (t, J=9.0 Hz, 1H), 7.15 (t, J=7.5 Hz, 1H), 7.22-7.29 (m, 1H), 7.38 (t, J=7.5 Hz, 1H); HPLC ES-MS m/z (rel abundance) 224 (MH+, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06784167B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-425daee0f1454325bdd44506ec458f77 |
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| Source note | uspto-grants-2004_08 |
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