HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → 5-Dimethylaminomethylfurfuryl chloride hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | ((2-(Hydroxymethyl)-5-furyl)methyl)ammonium chloride | HCID 3086123 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Dimethylaminomethylfurfuryl chloride hydrochloride | HCID 12954792 | — |
Reaction Steps
Combine 5-[(dimethylamino)methyl]-furfuryl alcohol hydrochloride (201 g, 1.05 mol) and acetonitrile (500 mL). Add dropwise, thionyl chloride (119 g, 1.0 mol) at such a rate that the temperature of the reaction is maintained at about 30° C. to 35° C. After the addition of thionyl chloride is complete, add methanesulfonic acid (144 g, 1.5 mol) while removing sulfur dioxide and acetonitrile by distillation. Stop the distillation when about 250 mL of distillate has been collected to give the title compound as a solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05672724 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-88d0520323934382803a9e351b4cb7bb |
| Source note | uspto-grants-1997_09 |