Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 5-((Dimethylamino)methyl)-2-furanmethanol | HCID 84906 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | ((2-(Hydroxymethyl)-5-furyl)methyl)ammonium chloride | HCID 3086123 | — |
Reaction Steps
In a device shown in FIG. 2, 38.5 kg/hr of aqueous 36 wt% hydrochloric acid solution was fed through a conduit 2 and 13.0 kg/hr of 5-(dimethylamino)methylfurfuryl alcohol was fed through a conduit 3 to a reactor 1 maintained at a temperature of 20° to 30° C. Aqueous hydrochloric acid solution of 5-(dimethylamino)methylfurfuryl alcohol hydrochloride thus obtained was continuously fed to a reactor 5 through a conduit 4. Under maintaining a temperature of the reactor at 50° to 60° C., 13.3 kg/hr of an aqueous 75 wt% cysteamine hydrochloride solution was continuously fed to the reactor 5 through a conduit 6. Further, a reaction product was continuously discharged from the reactor 5 through a conduit 7. Residence time at the reactor 1 was 10 minutes and the residence time at the reactor was 30 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04785122 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-5f12953ee4bb4ed6ac844c1c6af788b1 |
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| Source note | uspto-grants-1988_11 |
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