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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-((Dimethylamino)methyl)-2-furanmethanol | HCID 84906 | — |
| Reactant | HCID 178482512 | HCID 178482512 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 178482515 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04374248 |
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| Source dataset | uspto-grants-1983_02 |
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| ORD ID | ord-b215112212734fd6a1aa9c794656612c |
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| Source note | uspto-grants-1983_02 |
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