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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277995Generated: October 31, 2026

Methanesulfonic Acid → HCID 19750881, compound

https://huagongshe.com/reaction/1277995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant3-Amino-1-propanolHCID 9086—
ReactantSodium CarbonateHCID 10340—
Reactant5-((Dimethylamino)methyl)-2-furanmethanolHCID 84906—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 19750881HCID 1975088143.4%

Reaction Steps

To a stirred solution of methanesulphonic acid (18 ml) in dry tetrahydrofuran (40 ml) kept at room temperature was added, with stirring, a mixture of 5-[(dimethylamino)methyl]-2-furanmethanol (4.65 g) and 3-amino-1-propanol (6.75 g). After 3 days the suspension was heated on a steam bath for 30 mins. Excess anhydrous sodium carbonate and ethyl acetate (100 ml) were added and the heating continued for 20 mins. The hot suspension was filtered and the residue washed with hot ethyl acetate (3×50 ml). The combined filtrates were evaporated to dryness, water (150 ml) added and the solution extracted with ethyl acetate (3×50 ml). The aqueous fraction was acidified with oxalic acid (5 g) and the solution evaporated to low bulk. Ethyl acetate (100 ml) and excess anhydrous sodium carbonate were added and the suspension heated to boiling point for 30 mins. The hot suspension was filtered and the combined filtrates and washings evaporated to dryness. The oily residue was distilled (100°-110°/0.2 mm) to give the title compound (2.76 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04279911
Source datasetuspto-grants-1981_07
ORD IDord-c1efe522a34d432d9b65c590dd3d2229
Source noteuspto-grants-1981_07