HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751677Generated: October 28, 2026
Sodium Bromide → tert-butyl (2S,5S)-2-formyl-5-methylpyrrolidine-1-carboxylate
https://huagongshe.com/reaction/1751677
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (2S,5S)-tert-butyl 2-(hydroxymethyl)-5-methylpyrrolidine-1-carboxylate | HCID 12995944 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Catalyst | Tempo | HCID 2724126 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-butyl (2S,5S)-2-formyl-5-methylpyrrolidine-1-carboxylate | HCID 86688350 | 77% |
Reaction Steps
To a solution of (2S,5S)-tert-butyl 2-(hydroxymethyl)-5-methylpyrrolidine-1-carboxylate (5.15 g, 23.9 mmol) in dichloromethane, was added TEMPO (0.075 g, 0.48 mmol), sodium bromide (0.246 g, 2.39 mmol) and sodium bicarbonate (0.442 g, 5.26 mmol). Sodium hypochlorite (2.67 g, 35.9 mmol) of a 6% solution was added and the biphasic mixture was vigorously stirred for 2 hours at room temperature. The reaction mixture was extracted two times with dichloromethane (2×100 mL). The organic layers were combined and washed with saturated sodium thiosulfate solution, dried with sodium sulfate and the solvent was removed in vacuo to yield (2S,5S)-tert-butyl 2-formyl-5-methylpyrrolidine-1-carboxylate (3.9 g, 18.29 mmol, 77%) as a slight colored oil and was used directly in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156823B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-36beba21b8044aa6b54983b12d0f793a |
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| Source note | uspto-grants-2015_10 |
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