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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468192Generated: November 1, 2026

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

https://huagongshe.com/reaction/1468192

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, 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 numberUS09000191B2
Source datasetuspto-grants-2015_04
ORD IDord-8f1940349abd41b2b5f39b9645794f88
Source noteuspto-grants-2015_04