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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962631Generated: October 31, 2026

Water → 3-Benzyl-8-methoxy-1,2,3,4-tetrahydro-chromeno[3,4-c]pyridin-5-one

https://huagongshe.com/reaction/962631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-MethoxyphenolHCID 9007—
ReactantAmmonium HydroxideHCID 14923—
ReactantMethyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochlorideHCID 107479—
SolventSulfuric AcidHCID 1118—
Product3-Benzyl-8-methoxy-1,2,3,4-tetrahydro-chromeno[3,4-c]pyridin-5-oneHCID 988358747.1%

Reaction Steps

A mixture of 3-methoxyphenol (28.3 g, 227 mmol) and methyl 1-benzyl-4-oxo-3-piperidinecarboxylate hydrochloride (46.1 g, 162 mmol) is cooled in ice and treated dropwise with a solution prepared from 38 mL of water diluted to 150 mL with concentrated sulfuric acid. The mixture is stirred at room temperature for 48 hours, then added slowly to 500 g of ice and 100 mL of concentrated ammonium hydroxide. Additional ice and ammonium hydroxide are added until the pH of the mixture is 10 to 11. Stirring is continued until the initially gummy precipitate becomes granular. The solid is filtered, then stirred in 400 mL of 2.5% aqueous sodium hydroxide solution followed by 400 mL of 10% methanol in water. The solid is again filtered and recrystallized from 2-propanol to yield 24.5 g (47%) of final product; mp 118°-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05760050
Source datasetuspto-grants-1998_06
ORD IDord-fa26d66f7ec6403fb40b810203daa152
Source noteuspto-grants-1998_06