HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411959Generated: October 31, 2026
Hydrochloric Acid → HCID 178443806, compound
https://huagongshe.com/reaction/411959
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 11096866 | HCID 11096866 | — |
| Reactant | HCID 11810633 | HCID 11810633 | — |
| Reactant | HCID 178419078 | HCID 178419078 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178443806 | HCID 178443806 | 63% |
Reaction Steps
30 g of N-octyloxycarbonyl-β-alanine were dissolved in 300 ml of dimethylformamide and 1 molar equivalent of triethylamine. Next, 1 molar equivalent of 2-(5-norbornene-2,3-dicarboximido)-1,1,3,3-tetramethyluronium tetrafluoroborate was added. The mixture was then stirred for 1 hour at a temperature of 250° C. Next, a solution containing 1.2 molar equivalents of histidine and 1.2 molar equivalents of sodium hydroxide in 100 ml of water were added dropwise, while keeping the temperature below 30° C. After stirring for 6 hours, the mixture was neutralized with 1 molar equivalent of 5N hydrochloric acid, followed by 100 ml of water. After stirring for 30 minutes, the mixture was poured into 2 liters of acetone. The white precipitate formed was filtered off and dried. The crude product was dissolved in 10 ml/g of refluxing 96% ethanol. The solution was filtered while hot and the product then crystallized at room temperature. After processing the precipitate, 29.4 g of a white crystalline product were obtained (63% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562789B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-d066212d4a474289a0f83265b12131af |
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| Source note | uspto-grants-2003_05 |
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