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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267957Generated: October 25, 2026

Phenol → 1,2,3,4-Tetrahydro-5H-[1]benzopyrano[3,4-c]pyridin-5-one

https://huagongshe.com/reaction/267957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantSulfuric AcidHCID 1118—
ReactantAmmonium HydroxideHCID 14923—
Reactant3-Piperidinecarboxylic acid, 4-oxo-, ethyl ester, hydrochloride (1:1)HCID 107315—
SolventChloroformHCID 6212—
Product1,2,3,4-Tetrahydro-5H-[1]benzopyrano[3,4-c]pyridin-5-oneHCID 13136922—

Reaction Steps

A mixture of 18.8 g (0.2 m) of phenol and 20.7 g (0.1 m) of 3-carbethoxy-4-piperidone HCl was cooled in an ice bath and treated with 75 cc of 73% v/v H2SO4 in 1/2 hr. with stirring and protection from moisture. After stirring 4 days at room temperature the reaction was chilled and treated with an additional 10 g (0.106 m) of phenol. After 5 days a second 10 g portion of phenol was added. After stirring 6 days the reaction was treated with 100 g of ice and conc. NH4OH to pH 8-9. The resultant gum was stirred with 100 cc CHCl3 for 1/2 hr. and was filtered. The filtrate was evaporated and the resultant gum was triturated with pet ether followed by ethyl ether. The resultant solid was crystallized from 100 cc 3N HCl affording 2.3 g (10%) of product mp. 330°- 5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03946008
Source datasetuspto-grants-1976_03
ORD IDord-cb4cc3175ac8448fa4c0213be60c57ae
Source noteuspto-grants-1976_03