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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224550Generated: October 30, 2026

Pyridine → HCID 22812919, compound

https://huagongshe.com/reaction/224550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 22812922HCID 22812922—
SolventDichloromethaneHCID 6344—
ProductHCID 22812919HCID 22812919—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of diphenylmethyl α-[4(R)-acetonyloxy-3(R)-phenylacetamido-2-oxo-azetidin-1-yl]glycolate (2.136 g) in anhydrous methylene chloride (20 ml) are added thionyl chloride (0.90 ml) and pyridine (0.33 ml) with stirring at 0° C. After stirring for 1 hour at 0° C., the mixture is poured into ice water, and extracted with ethyl acetate. The organic layer is washed with water, dried over sodium sulfate, and evaporated under reduced pressure to give the crude product of a mixture of epimers at position α.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04233216
Source datasetuspto-grants-1980_11
ORD IDord-cac1d3303a4c42aa9299ffbecee3121a
Source noteuspto-grants-1980_11