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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15152Generated: October 25, 2026

2-Mercaptoethanol → 2-[(3,6-Dichloro-4-pyridazinyl)thio]ethanol

https://huagongshe.com/reaction/15152

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MercaptoethanolHCID 1567—
ReactantDichloromethaneHCID 6344—
Reactant3,4,6-TrichloropyridazineHCID 95123—
ReactantSodium BicarbonateHCID 516892—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Product2-[(3,6-Dichloro-4-pyridazinyl)thio]ethanolHCID 81766083—

Reaction Steps

A solution of 3,4,6-trichioropyridazine (25 g) in tetrahydrofuran (200 ml) and triethylamine (19 ml) was treated at 0° C. (ice bath cooling) with 2-mercaptoethanol (8.33 ml) over 5 minutes. After the addition was complete, the mixture was stirred at room temperature for 72 hours. The mixture was stirred with aqueous sodium bicarbonate solution and dichloromethane and the solid was collected, washed with water, ether and pentane and dried in vacuo, giving (22.9 g). The combined aqueous and organic fraction was evaporated to half volume giving further solid, which was washed and dried as above (5.0 g). The total yield of solid (27.9 g; 91%) contained some bromo-analogue (5-10%) by NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732460B2
Source datasetuspto-grants-2010_06
ORD IDord-ac95521bbf7746a397c2d885666fc1aa
Source noteuspto-grants-2010_06