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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649093Generated: October 31, 2026

Phosgene → HCID 12805020, compound

https://huagongshe.com/reaction/1649093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantCyclopropanemethanolHCID 75644—
ReactantIci 109,081HCID 161928—
ReactantCyclopropylmethyl carbonochloridateHCID 15917591—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 12805020HCID 1280502034%

Reaction Steps

3.2 g (44.4 millimoles) of (hydroxymethyl)cyclopropane, dissolved in 50 ml of absolute ether, are added dropwise to a stirred solution of 8.8 g (89.0 millimoles) of phosgene in 50 ml of absolute ether at 10°-15° C. The reaction solution is then stirred for 3 hours at room temperature. The excess phosgene is removed by means of a dry stream of nitrogen, and the ether is then removed under reduced pressure at room temperature. The cyclopropylmethyl chloroformate which remains is mixed with 6.0 g (29.5 millimoles) of 6-(p-aminophenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone and 100 ml of absolute toluene and the mixture is kept for 7 hours at 80° C. The product is filtered off at 10° C., washed first with toluene and then with water, and recrystallized twice from dimethylformamide/water. 3.0 g (34% of theory) of 6-(p-cyclopropylmethoxycarbonylaminophenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone are obtained as colorless crystals of melting point 240°-241° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04415571
Source datasetuspto-grants-1983_11
ORD IDord-9253a864865c4ca0827182453f9db111
Source noteuspto-grants-1983_11