HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587992Generated: October 28, 2026
Potassium Bromide → (S)-tert-butyl 3-formylpyrrolidine-1-carboxylate
https://huagongshe.com/reaction/587992
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | tert-butyl (3S)-3-(hydroxymethyl)pyrrolidine-1-carboxylate | HCID 1514341 | — |
| Reactant | Tempo | HCID 2724126 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | (S)-tert-butyl 3-formylpyrrolidine-1-carboxylate | HCID 1514343 | 75.7% |
Reaction Steps
To a solution of (S)-3-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester (4.0 g, 19.9 mmol, 1.0 eq.) in DCM was added TEMPO (62 mg, 0.4 mmol, 0.02 eq.) and potassium bromide (120 mg, 1.0 mmol, 0.05 eq.). The resulting mixture was cooled over ice (and a small amount of salt, −4° C.). A 1:1 mixture of 0.7M sodium hypochlorite in water and saturated NaHCO3 (56 mL total) was added dropwise. The resulting mixture was allowed to stand in the ice bath until layers separated (˜5 minutes). The layers were separated and extracted with DCM (3×30 mL). The organic layer was washed with water (30 mL) and saturated aqueous NaCl (30 mL), then dried over anhydrous Na2SO4, filtered and concentrated to yield (S)-3-formylpyrrolidine-1-carboxylic acid t-butyl ester (3.0 g), which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227933B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-6b2d948728354719b0afdc9ea179fa37 |
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| Source note | uspto-grants-2016_01 |
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