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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587992Generated: October 28, 2026

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

https://huagongshe.com/reaction/587992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
Reactanttert-butyl (3S)-3-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 1514341—
ReactantTempoHCID 2724126—
ReactantSodium HypochloriteHCID 23665760—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product(S)-tert-butyl 3-formylpyrrolidine-1-carboxylateHCID 151434375.7%

Reaction Conditions

Temperature-4 °C

Reaction Steps

To a solution of (S)-3-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester (4.0 g, 19.9 mmol, 1.0 eq.) in DCM was added TEMPO (62 mg, 0.4 mmol, 0.02 eq.) and potassium bromide (120 mg, 1.0 mmol, 0.05 eq.). The resulting mixture was cooled over ice (and a small amount of salt, −4° C.). A 1:1 mixture of 0.7M sodium hypochlorite in water and saturated NaHCO3 (56 mL total) was added dropwise. The resulting mixture was allowed to stand in the ice bath until layers separated (˜5 minutes). The layers were separated and extracted with DCM (3×30 mL). The organic layer was washed with water (30 mL) and saturated aqueous NaCl (30 mL), then dried over anhydrous Na2SO4, filtered and concentrated to yield (S)-3-formylpyrrolidine-1-carboxylic acid t-butyl ester (3.0 g), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227933B2
Source datasetuspto-grants-2016_01
ORD IDord-6b2d948728354719b0afdc9ea179fa37
Source noteuspto-grants-2016_01