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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1153915Generated: November 1, 2026

Ethanol → HCID 178442730, compound

https://huagongshe.com/reaction/1153915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium AzideHCID 33557—
ReactantPiperidine, 1-methyl-, hydrochlorideHCID 205378—
ReactantHCID 19848841HCID 19848841—
CatalystN-MethylpiperidineHCID 12291—
ProductHCID 178442730HCID 178442730—

Reaction Steps

Finely ground sodium azide (325 mg, 5 mmole) is added to a solution of 5-acetoxy-4-cyano-2,2-dimethyl-7-(1,1-dimethylheptyl)-3,4-dihydro-2H-benzopyran (1.855 g, 5 mmole) in 10 ml ethanol-free chloroform containing 271 mg (2 mmole) N-methylpiperidine hydrochloride and 5 drops of N-methylpiperidine. The mixture is heated at reflux for one hour, another 2 mmoles of N-methylpiperidine hydrochloride is added, refluxing is continued for one hour and the mixture is allowed to stand overnight at room temperature. The mixture is partitioned between chloroform and aqueous sodium carbonate solution, the aqueous phase is adjusted to pH 5 and extracted again with chloroform. The combined organic layers are washed with water, dried (MgSO4) and the solvent evaporated in vacuo to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04486428
Source datasetuspto-grants-1984_12
ORD IDord-cda9c3f2322b43f8901cf82a0df219f0
Source noteuspto-grants-1984_12