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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371932Generated: October 30, 2026

Hydrochloric Acid → (+/-)-6-(4'-Butanoyloxyphenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone

https://huagongshe.com/reaction/2371932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantButyryl chlorideHCID 8855—
Reactant6-(4-Hydroxyphenyl)-5-methyl-4,5-dihydropyridazin-3(2H)-oneHCID 135542478—
SolventPyridineHCID 1049—
Product(+/-)-6-(4'-Butanoyloxyphenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinoneHCID 1501640580%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 100 ml round-bottomed flash was charged with pyridine (30 ml) and 7.10 g (34.8 mmol) of (±)-4,5-dihydro-6-(4'-hydroxyphenyl)-5-methyl-3(2H)-pyridazinone from Example I, then cooled to 0° C. under an atmosphere of nitrogen. Butanoyl chloride (4.10 g, 38.3 mmol) was added dropwise to the solution via syringe. The reaction mixture was stirred for 30 min at 0° C., warmed to 23° C. over 15 min then poured into 1N aqueous hydrochloric acid (400 ml). The aqueous solution was extracted with EtOAc (2×200 ml). The combined EtOAc extracts were successively washed with 5% aqueous sodium bicarbonate solution (300 ml), saturated aqueous sodium chloride (200 ml), dried over anhydrous magnesium sulfate (5 g), filtered and concentrated in vacuo to provide 9.8 g of crude product as a solid. Recrystallization from ethyl acetae/hexanes (2:1, 35 ml) yielded 7.61 g (80%) of pure (±)-6-(4'-butanoyloxyphenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone as colorless needles, m.p. 112°-113° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05096904
Source datasetuspto-grants-1992_03
ORD IDord-aed2456f8a7f427492ed2103236bcbd8
Source noteuspto-grants-1992_03