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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059029Generated: November 3, 2026

Dihydrocoumarin → Cyclohexadienone, hydroxy-

https://huagongshe.com/reaction/2059029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDihydrocoumarinHCID 660—
ReactantChloroformHCID 6212—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Product4-chloro-N-methylpiperidineHCID 79342—
ProductCyclohexadienone, hydroxy-HCID 44055446%

Reaction Steps

The Grignard reagent of 4-chloro-N-methylpiperidine (60 g, 0.47 moles) is prepared as in Example 3A. To this is added a solution of 23 g (0.155 moles) dihydrocoumarin in 100 ml tetrahydrofuran over 20 minutes (reaction is refluxed). Refluxed for 31/2 hours. The flask is cooled in an ice bath and saturated ammonium chloride solution is added (200 ml). The layers are separated and the aqueous extracted with tetrahydrofuran. The organics are dried (magnesium sulfate) and evaporated. The residue, after an acid-base extraction, yield 13 g from the organics. Carbon dioxide is bubbled through the aqueous which is then extracted with dichloromethane. These organics are dried and evaporated to yield 26 g. Chromatography (basic alumina, activity III, chloroform) afforded 17.7 g (46%) crystalline keto-phenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04321270
Source datasetuspto-grants-1982_03
ORD IDord-8a7ccf947c344df2913830ffdc8cf98a
Source noteuspto-grants-1982_03