HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900563Generated: October 30, 2026
Dimethyl Sulfoxide → 1-tert-butyl 2-methyl (2S)-4-oxopyrrolidine-1,2-dicarboxylate
https://huagongshe.com/reaction/900563
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1-(tert-butyl) 2-methyl (2S)-4-hydroxypyrrolidine-1,2-dicarboxylate | HCID 12185578 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-tert-butyl 2-methyl (2S)-4-oxopyrrolidine-1,2-dicarboxylate | HCID 10988485 | 89% |
Reaction Steps
To a solution of 9.63 mL (7.2 mmol) of oxalyl chloride in 10.6 mL of CH2Cl2 stirred at −78° C. was added a solution of 0.94 mL (13.2 mmol) of methyl sulfoxide in 15 mL of CH2Cl2. The solution was stirred at −78° C. for 30 min. A solution of 1.47 g (6 mmol) of N-Boc-4-hydroxyproline methyl ester in 19 mL of CH2Cl2 was then added dropwise. The mixture was stirred at −78° C. for 1.5 h, and 3.34 mL (24 mmol) of triethylamine was added. The solution was allowed to warm up to room temperature and stirred overnight. It was then diluted with 100 mL of CH2Cl2, washed successively with 100 mL of water, 100 mL of 1N HCl, and 100 mL of brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography over silica gel (eluted with ethyl acetate/hexanes, 1:3), to afford 1.294 g (89% yield) of N-Boc-4-oxo-proline methyl ester. 1H NMR (500 MHz, CDCl3) δ 1.45 (m, 9H), 2.60 (m, 1H), 2.95 (m, 1H), 3.75 (m, 3H), 3.90 (m, 2H), 4.80 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07358273B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-f0a2efcf9b9b47a89a2da441f3eb0973 |
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| Source note | uspto-grants-2008_04 |
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