HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374536Generated: October 30, 2026
Dimethyl Sulfoxide → Tert-butyl 3-oxopyrrolidine-1-carboxylate
https://huagongshe.com/reaction/1374536
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Boc-3-pyrrolidinol | HCID 4416939 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 3-oxopyrrolidine-1-carboxylate | HCID 471360 | 97.2% |
Reaction Steps
Part A: To a solution of oxalyl chloride (1.3 mL, 15 mmol) in 20 mL of dichloromethane at −60° C. was added methyl sulfoxide dropwise over period of 10 min. After stirring at −60° C., a solution of 1,1-dimethylethyl 3-hydroxypyrrolidine-1-carboxylate (1.87 g, 10 mmol) in 20 mL of dichloromethane was added over 20 min. Then, diisopropylethylamine (8.8 mL, 50 mmol) was added over 5 min. The resulting mixture was stirred at −60° C. for 25 min, and at room temperature for 30 min. The reaction was diluted with dichloromethane (100 mL). The organic layer was washed sequentially with saturated sodium bisulfate solution (2×), saturated sodium bicarbonate solution, water, and brine; dried over sodium sulfate; and concentrated to afford 1.8 g (97%) of 1,1-dimethylethyl 3-oxo-pyrrolidine-1-carboxylate: 1H-NMR (CDCl3) δ 3.75 (4H, m), 2.58 (2H, t, J=7.8 Hz), 1.49 (9H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07166586B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-d56a2b0a4bce4528b1b5cd713fa7aeb3 |
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| Source note | uspto-grants-2007_01 |
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