Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758614Generated: October 26, 2026

5-((Dimethylamino)methyl)-2-furanmethanol → HCID 178482515, compound

https://huagongshe.com/reaction/1758614

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-((Dimethylamino)methyl)-2-furanmethanolHCID 84906—
ReactantHCID 178482512HCID 178482512—
SolventHydrochloric AcidHCID 313—
ProductHCID 178482515HCID 178482515—

Reaction Steps

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°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04374248
Source datasetuspto-grants-1983_02
ORD IDord-b215112212734fd6a1aa9c794656612c
Source noteuspto-grants-1983_02