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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

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 numberUS09156823B2
Source datasetuspto-grants-2015_10
ORD IDord-36beba21b8044aa6b54983b12d0f793a
Source noteuspto-grants-2015_10