Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-(hydroxyMethyl)-5-Methyl-2-Pyrrolidinone | HCID 84072735 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 86714588 | HCID 86714588 | — |
Reaction Steps
A 50 mL flask was charged with 5-(hydroxymethyl)-5-methylpyrrolidin-2-one (646 mg, 5 mmol), purged with nitrogen, and dry 1,2-dichloroethane (10 mL) and pyridine (1.8 mL, 22.5 mmol, 4.5 equiv.) were added. Neat thionyl chloride (1.8 mL, 25 mmol, 5 equiv.) was added dropwise over 10 min, during which the suspension clarified briefly before becoming a thick slurry. The mixture was stirred at room temperature for 30 min, then heated to reflux. After 3.5 h, the cooled mixture was concentrated to an orange semi-solid, which was absorbed on silica. Chromatography on silica (50-100% EtOAc/hexane) afforded the title compound as a colorless oil which solidified on standing (383 mg, 52%). 1H NMR (400 MHz, CDCl3) δ 6.48 (br s, 1H), 3.52 (s, 2H), 2.56-2.41 (m, 2H), 2.15 (ddd, J=6.0, 9.4, 15.4 Hz, 1H), 1.98 (ddd, J=7.9, 9.4, 17.3 Hz, 1H), 1.42 (s, 3H); LRMS (ESI/APCI): 148 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729112B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-474ca3fccffd4916b9e62d6263bcbf94 |
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| Source note | uspto-grants-2014_05 |
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