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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244923Generated: October 31, 2026

Potassium Bromide → (S)-tert-butyl 3-formylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/244923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-butyl (3S)-3-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 1514341—
ReactantSodium HypochloriteHCID 23665760—
CatalystTempoHCID 2724126—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(S)-tert-butyl 3-formylpyrrolidine-1-carboxylateHCID 151434387%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of (S)-3-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester (25.0 g, 124 mmol, 1.0 eq.) in DCM (200 mL) was cooled with stirring to 0° C. A solution of potassium bromide (1.5 g, 12.4 mmol, 0.1 eq.) and sodium bicarbonate (1.5 g, 17.4 mmol, 0.14 eq.) dissolved in water (100 mL) was added. After 15 minutes of stirring at 0° C., TEMPO (195.3 mg, 1.2 mmol, 0.01 eq.) was added, followed by the slow addition of sodium hypochlorite (77.3 mL, 136.6 mmol, 1.1 eq.) dropwise keeping the internal temperature in the 6-8° C. range. The mixture was placed in an ice bath until the layers separated. The organic layer was separated and the aqueous layer was extracted with DCM (200 mL). The combined organic layers were washed with saturated aqueous NaCl (200 mL), dried over Na2SO4, filtered, and concentrated to yield crude (S)-3-formylpyrrolidine-1-carboxylic acid t-butyl ester (21.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658691B2
Source datasetuspto-grants-2014_02
ORD IDord-3d29b83756bf4520a32f5de96d5cc002
Source noteuspto-grants-2014_02