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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262700Generated: October 25, 2026

Pyridine → N-Nitroso-L-proline

https://huagongshe.com/reaction/262700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantL-ProlineHCID 145742—
ReactantNitrilooxonium tetrafluoroborateHCID 11137142—
SolventAcetonitrileHCID 6342—
ProductN-Nitroso-L-prolineHCID 10419304—

Reaction Steps

To a cooled suspension of 28.2 g. of nitrosyl tetrafluoroborate in 300 ml. of dry acetonitrile there is added, with vigorous stirring, over the course of 10 minutes, 18.4 g. of L-proline, followed by a solution of 19 g. of pyridine in 50 ml. of acetonitrile during 15 minutes. The stirring is continued for an hour and the reaction mixture is then concentrated to dryness under reduced pressure. The residue is extracted with 3×200 ml. of ethyl acetate, the ethyl acetate extracts are combined, washed twice with saturated sodium chloride solution that has been made slightly acidic with concentrated hydrochloric acid. The ethyl acetate solution is dried over anhydrous sodium sulfate, filtered and concentrated to dryness at room temperature under reduced pressure. The product, N-nitroso-L-proline metls at 108°-109° (dec.) after crystallization from a mixture of ether and petroleum ether (30°-60°).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04154934
Source datasetuspto-grants-1979_05
ORD IDord-f743446f9c7647f482d8b7ba7cee7e0a
Source noteuspto-grants-1979_05