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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253515Generated: November 2, 2026

Pyridine → (+-)-1-(tert-Butoxycarbonyl)pyrrolidine-3-carboxaldehyde

https://huagongshe.com/reaction/1253515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactanttert-Butyl 3-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 5237175—
Catalystchromium (VI) trioxideHCID 10219390—
SolventDichloromethaneHCID 6344—
Product(+-)-1-(tert-Butoxycarbonyl)pyrrolidine-3-carboxaldehydeHCID 4692112—

Reaction Steps

To a solution of pyridine (9.5 g, 0.12 mol) in dichloromethane (150 mL) was added chromium trioxide (6.0 g, 0.06 mol). The internal reaction temperature was not allowed to exceed 20° C. during the addition. After 15 minutes, the stirred mixture was charged with a solution of tert-butyl 3-(hydroxymethyl)pyrrolidine-1-carboxylate (2.0 g, 10 mmol) in dichloromethane (30 mL). After 15 minutes, the solution was decanted from the reaction vessel which was washed with dichloromethane (200 mL). The organics were combined, washed with 5% aqueous sodium hydroxide (3×100 mL), then washed with 5% hydrochloric acid (100 mL), then washed with 5% aqueous sodium bicarbonate (100 mL), and finally washed with 5% aqueous sodium chloride (100 mL). The organics were dried over magnesium sulfate, filtered, and concentrated in vacuo to afford tert-butyl 3-formylpyrrolidine-1-carboxylate that was used without additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455477B2
Source datasetuspto-grants-2013_06
ORD IDord-c9eb831ad1504dbf8ff82468b344d09c
Source noteuspto-grants-2013_06