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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568309Generated: October 30, 2026

Triethylamine → HCID 14099148, compound

https://huagongshe.com/reaction/568309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenyl chloroformateHCID 15891—
Reactant5,6-dichloropyridazin-4-amineHCID 6403202—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14099148HCID 1409914826.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred suspension of 2.0 grams (0.012 mole) of 4-amino-5,6-dichloropyridazine in 75 ml of tetrahydrofuran is cooled to 0° C. and 1.5 grams (0.015 mole) of triethylamine is added in one portion. A solution of 2.3 grams (0.015 mole) of phenyl chloroformate in tetrahydrofuran is added dropwise during a 30 minute period. Upon completion of addition the reaction mixture is allowed to warm to ambient temperature where it is stirred for three days. The reaction mixture is taken up in 500 ml of chloroform and filtered to collect 0.98 gram of phenyl N-(5,6-dichloro-4-pyridazinyl)carbamate. The filtrate is concentrated under reduced pressure to a residue. The residue is subjected to column chromatography on silica gel to yield an additional 0.9 gram of phenyl N-(5,6-dichloro-4-pyridazinyl)carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04728355
Source datasetuspto-grants-1988_03
ORD IDord-29e4c381e0664089b140c5a870c3b051
Source noteuspto-grants-1988_03