HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679261Generated: October 29, 2026
Hydrochloric Acid → HCID 178479081, compound
https://huagongshe.com/reaction/1679261
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | 2-Acetamidopyridine | HCID 72929 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178479081 | HCID 178479081 | — |
Reaction Steps
The solution of 2-acetamidopyridine was chilled in an ice bath to 10°-15° C and treated with 118 g. of commercial 40% peracetic acid which was slowly added over a 40-minute period with ice-cooling and stirring. During the course of the addition the temperature was between 15°-25° C. After 1 hour stirring, with little cooling (temperature 20°-30° C), the turbid solution was heated for 3.5 hours at 70° C with stirring. To the clear hot solution were added 85 g. 37.5% hydrochloric acid and 37 g. water, and to the resulting cloudy solution was added 3.5 g. 37% formaldehyde solution to destroy any unreacted excess of peroxide compounds. The mixture was stirred and heated 2.5 hours at 80°-82° C. After cooling to room temperature, 40 g. xylene was added and the cloudy solution was evaporated, under vacuum, in a rotary evaporator, until the residue was solid. The resulting moist crystals were dried at 50°-60° C under vacuum, to give 116 g. of 2-aminopyridine-1-oxide hydrochloride, which on recrystallization from 1:1 ethanoltoluene mixture, weighed 98.8 g. The resulting colorless crystals gave a m.p. of 155°-156° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04080329 |
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| Source dataset | uspto-grants-1978_03 |
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| ORD ID | ord-83e37178c5d240f0b1c18a4826a2573c |
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| Source note | uspto-grants-1978_03 |
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