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HRID 1758614作成日:2026年10月26日

5-((Dimethylamino)methyl)-2-furanmethanol → HCID 178482515、化合物

https://huagongshe.com/reaction/1758614

反応式

関与物質

役割名称HCID仕込み量
反応物5-((Dimethylamino)methyl)-2-furanmethanolHCID 84906—
反応物HCID 178482512HCID 178482512—
溶媒Hydrochloric AcidHCID 313—
生成物HCID 178482515HCID 178482515—

反応手順

A mixture containing 3-methylamino-4-(2-mercaptoethylamino)-1,2,5-thiadiazole 1,1-dioxide (1.0 g; 4.5 mmoles) [prepared in Step A] and 5-dimethylaminomethyl-2-furanmethanol (0.82 g; 4.5 mmoles) [prepared according to the procedure in J. Chem. Soc., 4728 (1958)] in 20 ml of concentrated hydrochloric acid was stirred in an ice-water bath for 2 hours and then allowed to stand at 0° for 64 hours. The reaction mixture was stirred at ambient temperature for 23 hours, evaporated without heating under reduced pressure and the residue partitioned between water and methylene chloride. The aqueous phase was made basic with sodium bicarbonate and extracted with methylene chloride. The combined organic phase was washed with saturated brine solution, dried and evaporated under reduced pressure. The residue was placed on 25 g of silica gel and chromatographed using a gradient elution of methylene chloride-methanol. The appropriate fraction was evaporated and the product crystallized from methanol. Recrystallization from methanol yielded the title compound, mp 92°-96°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04374248
出典データセットuspto-grants-1983_02
ORD IDord-b215112212734fd6a1aa9c794656612c
出典メモuspto-grants-1983_02