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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468196Generated: November 1, 2026

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

https://huagongshe.com/reaction/1468196

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 numberUS09000191B2
Source datasetuspto-grants-2015_04
ORD IDord-2a36b72d89a846a98cbfa45e42eb38c1
Source noteuspto-grants-2015_04