Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | HCID 178419078 | HCID 178419078 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68452512 | HCID 68452512 | 99% |
Reaction Steps
L-Histidine (204.8 g, 1.32 mol) was added to water (1.2 L) and cooled in an ice/water bath. Concentrated hydrochloric acid (116.0 mL, 1.39 mol, 1.05 mol eq.) was added slowly. Formaldehyde (37 wt/wt % in water, 112.5 g, 1.39 mol, 1.05 mol eq.) was added in one portion. The reaction mixture was stirred for 30 min upon cooling with an ice/water bath, and then refluxed for 75 min. After cooling to room temperature, the solvent was removed under reduced pressure. The residue was suspended in isopropanol (2 L) and HCl (400 mL of a 4 M solution in dioxane) for 30 min. The white solid was filtered and washed with ether. After drying in a vacuum oven (40° C.), the title product was obtained. (313.0 g, 99% yield, 95% pure). 1H NMR (DMSO-d6): 8 ppm 3.05-3.33 (m, 2H), 4.30 (s, 2H), 4.54 (m, 1H), 9.00 (s, 1H), 12.60 (br s, 3H). LCMS: Rt=0.59 min, and M+1=168.1 m/z (M+1 of free base).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468375B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-2799d526427a47d4bde68d9123660cb8 |
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| Source note | uspto-grants-2008_12 |
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