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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379394Generated: October 25, 2026

Triethylamine → HCID 86748235, compound

https://huagongshe.com/reaction/2379394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantS-Butyl carbonochloridothioateHCID 13295035—
ReactantHCID 178515449HCID 178515449—
SolventBenzeneHCID 241—
ProductHCID 86748235HCID 86748235—
ProductHCID 178516196HCID 178516196—

Reaction Steps

3-(4'-Chlorophenyl)-4-hydroxy-6-bromopyridazine (14.2 g, 0.0497 mol) was suspended in 100 ml of benzene, triethylamine (5.5 g, 0.0543 mol) was added, and the mixture was stirred for 3.5 hours at room temperature to complete the reaction. S-Butyl thiochlorocarbonate (7.85 g, 0.05162 mol) was then added dropwise to the mixture in the course of 5 minutes, and the reaction mixture was stirred for 3 more hours without heating. The triethylamine hydrochloride which had precipitated was filtered off, and the benzene solution was washed in succession in each case with 150 ml portions of water, highly dilute hydrochloric acid, highly dilute sodium hydroxide solution and then again water, and dried over sodium sulfate. The solvent was then removed completely in vacuo, and finally under an oil-pump vacuum (0.2 Torr, 90° C. bath temperature). The S-butyl thiocarbonate of 3-(4'-chlorophenyl)-4-hydroxy-6-chloropyridazine, which was first obtained as an oil (17.5 g, 0.04356 mol, 87.6% of theory), solidified upon prolonged standing and, when dissolved in and allowed to crystallize from hexane, showed amp. of 68°-71° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05362708
Source datasetuspto-grants-1994_11
ORD IDord-3266497d9faf4e908792c2687ff2706e
Source noteuspto-grants-1994_11