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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1412967Generated: October 30, 2026

Sodium Bromide → tert-butyl (2S,5S)-2-formyl-5-methylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1412967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BromideHCID 253881—
ReactantSodium BicarbonateHCID 516892—
Reactant(2S,5S)-tert-butyl 2-(hydroxymethyl)-5-methylpyrrolidine-1-carboxylateHCID 12995944—
ReactantSodium HypochloriteHCID 23665760—
CatalystTempoHCID 2724126—
SolventDichloromethaneHCID 6344—
Producttert-butyl (2S,5S)-2-formyl-5-methylpyrrolidine-1-carboxylateHCID 8668835077%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921341B2
Source datasetuspto-grants-2014_12
ORD IDord-922d20efd24b42ad879dc9f175755580
Source noteuspto-grants-2014_12