HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539936Generated: October 31, 2026
Dimethyl Sulfoxide → tert-butyl (2S)-2-formylpyrrolidine-1-carboxylate
https://huagongshe.com/reaction/539936
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | (S)-(-)-N-Boc-prolinol | HCID 643448 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-butyl (2S)-2-formylpyrrolidine-1-carboxylate | HCID 2734674 | 100.4% |
Reaction Steps
A 2 L, 3-necked round bottomed flask equipped with an overhead stir and a N2 inlet was charged with a solution of oxalyl chloride (130 mL, 0.26 mol) in DCM (250 mL). The solution was cooled to −78° C., and a solution of DMSO (20 mL, 0.28 mol) in DCM (30 mL) was added dropwise. After 30 minutes, a solution of (S)—N-Boc-prolinol (40 g, 0.20 mol) in DCM (200 mL) was added dropwise. After 30 minutes, TEA (140 mL, 1.00 mol) was added to the solution, and the flask was transferred to an ice/water bath and stirred for another 30 minutes. The reaction mixture was diluted with DCM (200 mL) and washed successively with H2O, 1M HCl, saturated NaHCO3, and brine. The DCM layer was dried over Na2SO4, filtered, and concentrated to afford crude (S)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester (40 g) as an oil, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871759B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-081762726027441aa10603c8a0222690 |
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| Source note | uspto-grants-2014_10 |
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