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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644819Generated: October 31, 2026

Triacetoxyperiodinane → 2-(4-Fluoro-phenyl)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1644819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriacetoxyperiodinaneHCID 159087—
Reactant2-(4-Fluoro-phenyl)-2-hydroxymethyl-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 66773577—
SolventDichloromethaneHCID 6344—
Product2-(4-Fluoro-phenyl)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 86635623106.6%

Reaction Steps

To 2-(4-fluoro-phenyl)-2-hydroxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (3.9 g) in a round bottom flask was added Dess-Martin periodinane solution (47 mL of a 15% solution in DCM, CAS [87413-09-0]) and the reaction mixture was stirred for 5 hours at RT. The reaction mixture was then quenched with saturated aqueous sodium thiosulfate solution (25 mL) and stirred a further 20 minutes. The phases were separated and the aqueous was extracted with further DCM (25 mL). The combined organic phases were washed with saturated sodium bicarbonate solution and dried over sodium sulfate. Filtration of the drying agent and evaporation of the volatiles in vacuo afforded the desired 2-(4-fluoro-phenyl)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester (4.13 g, MS (ES+): 294.1 (MH+)) as a brown solid which was taken into the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124636B2
Source datasetuspto-grants-2012_02
ORD IDord-0743f584853140efbd7affb7db0cec47
Source noteuspto-grants-2012_02