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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328036Generated: October 30, 2026

Water → HCID 19922029, compound

https://huagongshe.com/reaction/328036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantPyridinium chlorideHCID 10176127—
Reactant9-Methoxy-1,2-dihydro-3H-naphtho[2,1-b]pyran-3-oneHCID 19921988—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 19922029HCID 19922029—

Reaction Steps

A mixture of 2.57 g (11.3 mmol) of 1,2-dihydro-9-methoxy-3H-naphtho[2,1-b]pyran-3-one from the preceding example and 7.86 g (68.0 mol) of pyridine hydrochloride was heated at 200°-230° C. for 2.5 hr. After being cooled to room temperature, the reaction mixture was treated with 100 mL of water and worked-up with ethyl acetate in the usual manner. The crude product (2.52 g) was dissolved in 150 mL of toluene, treated with 0.31 g (1.63 mmol) of p-toluenesulfonic acid monohydrate, and the resulting solution was stirred at reflux for 3.5 hr, with removal of water using a Dean-Stark trap. The solution was diluted with 300 mL of ethyl acetate, washed three times with saturated sodium bicarbonate solution, and work-up was completed in the usual manner. The crude product was purified by flash chromatography on 300 g of silica gel, eluting with hexane-ethyl acetate (3:1) to give 2.06 g (85.3%) of the title compound as a light-brown solid, mp 194°-202° C. (recrystallized from ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05273999
Source datasetuspto-grants-1993_12
ORD IDord-71531ca0140047b9aa455d5bfe326dd4
Source noteuspto-grants-1993_12