HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248411Generated: October 30, 2026
Methanesulfonic Acid → HCID 86740155, compound
https://huagongshe.com/reaction/1248411
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Amino-1-butanol | HCID 25868 | — |
| Reactant | 5-((Dimethylamino)methyl)-2-furanmethanol | HCID 84906 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86740155 | HCID 86740155 | — |
Reaction Steps
A solution of methanesulphonic acid (86 g), 5-[(dimethylamino)methyl]-2-furanmethanol (15.52 g), and 4-aminobutanol (17.82 g) in tetrahydrofuran (100 ml) was heated at 98°-100° for 1.5 h. After 1 h. at room temperature, excess anhydrous sodium carbonate was added and the suspension filtered after 18 h. The filtrate was evaporated, water (230 ml) added and the suspension extracted with ether (3×80 ml). The ethereal extracts were washed with water (2×50 ml), the aqueous fraction acidified with oxalic acid (25 g) and evaporated to low bulk. Excess anhydrous sodium carbonate and ethyl acetate (200 ml) were added, the suspension heated at boiling for 30 min. and the suspension filtered after 2 h. Evaporation of the filtrate yielded an oil which was distilled (100°-110°/0.08 mm) to give the title compound (6.64 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04524071 |
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| Source dataset | uspto-grants-1985_06 |
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| ORD ID | ord-9ad6cdf99efc47b7bc35bec835250a93 |
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| Source note | uspto-grants-1985_06 |
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