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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543052Generated: October 25, 2026

Water → Phenyl 1-(4-Chlorophenyl)-1,4-dihydro-4-oxo-6-methylpyridazine-3-carboxylate

https://huagongshe.com/reaction/543052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenolHCID 996—
ReactantTriethylamineHCID 8471—
ReactantFenridazonHCID 197225—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductPhenyl 1-(4-Chlorophenyl)-1,4-dihydro-4-oxo-6-methylpyridazine-3-carboxylateHCID 919200619.1%

Reaction Steps

To an ice cooled suspension of 5.29 g (0.02 mol) 1-(4-chlorophenyl)-1,4-dihydro-4-oxo-6-methyl pyridazine-3-carboxylic Acid (see Example 12) and 2.02 g (0.02 mol) of triethylamine in 125 ml of toluene there is added dropwise 3.13 g (0.02 mol) of phenyl chlorofomate. The suspension formed is stirred at room temperature for 15 minutes and to it there is added 1.88 g (0.02 mol) of phenol in 25 ml of toluene. The mixture is stirred at room temperature for 18 hrs. and to it there is added 100 ml of water. The suspension is stirred at room temperature for 2 hrs. and is poured into 800 ml of hexane. The suspension formed is stirred at room temperature for 3 hrs. and is vacuum filtered. The filter cake is slurried in 25 ml of toluene and is filtered. The filtrate is added to 150 ml of hexane and the suspension formed is stirred at room temperature for 2 hrs. The suspension is vacuum filtered and the filter cake air dried to afford 1.3 g (19% yield) of product, mp 140°-146° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04661145
Source datasetuspto-grants-1987_04
ORD IDord-57e33cddfbd445fba7ba3ddce2647e99
Source noteuspto-grants-1987_04