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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371235Generated: October 31, 2026

Formic Acid → HCID 13478225, compound

https://huagongshe.com/reaction/371235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantPyridineHCID 1049—
ReactantSulfur trioxideHCID 24682—
ReactantHCID 15058003HCID 15058003—
SolventDichloromethaneHCID 6344—
ProductHCID 13478225HCID 13478225—

Reaction Steps

(S)-(trans)-4-ethynyl-2-oxo-3-[(triphenylmethyl)amino]azetidine (404 mg) and 560 mg of a complex of pyridine and sulfur trioxide are added to a 25 ml flask. After the flask is flushed with nitrogen, 4.0 ml of dry pyridine is added and the mixture is heated at 80°-85° C. for 3 hours. The mixture is added to a rapidly stirred mixture of 4.0 ml of concentrated hydrochloric acid, 50 ml of water, and 50 ml of ethyl acetate. The pH is adjusted to 3.15 with sodium carbonate. The water layer is separated and extracted once with ethyl acetate. The combined organic layer is washed once with saturated aqueous sodium chloride, dried over sodium sulfate and filtered. Solvent removal in vacuo gives a foam which is taken up in 10 ml of dichloromethane. Formic acid (98%, 8 ml) is added, and after 15 minutes the mixture is concentrated to 4 ml and 10 ml of dichloromethane is added to give a solid suspended in solution. Filtration gives 100 mg of the title compound as a solid (obvious discoloration with melting >180° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04529698
Source datasetuspto-grants-1985_07
ORD IDord-9c4bc837e41941968418eac969016fc1
Source noteuspto-grants-1985_07