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HRID 15152作成日:2026年10月26日

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

https://huagongshe.com/reaction/15152

反応式

関与物質

役割名称HCID仕込み量
反応物2-MercaptoethanolHCID 1567—
反応物DichloromethaneHCID 6344—
反応物3,4,6-TrichloropyridazineHCID 95123—
反応物Sodium BicarbonateHCID 516892—
溶媒TetrahydrofuranHCID 8028—
溶媒TriethylamineHCID 8471—
生成物2-[(3,6-Dichloro-4-pyridazinyl)thio]ethanolHCID 81766083—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732460B2
出典データセットuspto-grants-2010_06
ORD IDord-ac95521bbf7746a397c2d885666fc1aa
出典メモuspto-grants-2010_06