Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026174Generated: November 1, 2026

Sodium Bromide → tert-butyl (3R)-3-formylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/1026174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BromideHCID 253881—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl (3R)-3-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 1514340—
ReactantSodium HypochloriteHCID 23665760—
CatalystTempoHCID 2724126—
SolventDichloromethaneHCID 6344—
Producttert-butyl (3R)-3-formylpyrrolidine-1-carboxylateHCID 1514342101%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of (R)-3-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester (50.0 g, 248.4 mmol, 1.0 eq.) in DCM (883 mL) was combined with TEMPO (1.9 g, 12.4 mmol, 0.05 eq.) and sodium bromide (2.6 g, 24.8 mmol, 0.1 eq.). The solution was cooled to 0° C. A solution of sodium hypochlorite (272.1 mL, 1.5 eq.) and sodium bicarbonate (31.2 g, 1.5 eq.) was added. Upon completion of the reaction, the mixture was extracted with DCM (3×200 mL) and dried over Na2SO4, to yield (R)-3-formylpyrrolidine-1-carboxylic acid t-butyl ester (50 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729119B2
Source datasetuspto-grants-2014_05
ORD IDord-8a6d22aae3994f749016b4337dcad6c0
Source noteuspto-grants-2014_05