HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286659Generated: October 27, 2026
Hydrochloric Acid → 2-(6-Formamidopyridin-2-yl)-2-propoxyiminoacetic acid
https://huagongshe.com/reaction/2286659
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | O-propylhydroxylamine hydrochloride | HCID 12283955 | — |
| Reactant | S-methyl 2-(6-formamidopyridin-2-yl)thioglyoxylate | HCID 13060226 | — |
| Reactant | 2-(6-Formamidopyridin-2-yl)glyoxylic acid | HCID 19790165 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(6-Formamidopyridin-2-yl)-2-propoxyiminoacetic acid | HCID 53664791 | — |
Reaction Steps
A mixture of S-methyl 2-(6-formamidopyridin-2-yl)thioglyoxylate (4.48 g.), methanol (20 ml.) and 1 N aqueous solution of sodium hydroxide (20 ml.) was stirred for 50 minutes at ambient temperature to give a solution containing 2-(6-formamidopyridin-2-yl)glyoxylic acid. To the solution was added O-propylhydroxylamine hydrochloride (2.23 g.), and the mixture was stirred for 35 minutes at the same temperature. The reaction mixture was adjusted to pH 7 with hydrochloric acid and the methanol was distilled off. The remaining aqueous mixture was washed with ethyl acetate, and ethyl acetate was added thereto and then adjusted to pH 1 with 10% hydrochloric acid. The ethyl acetate layer was separated, washed with water, dried over magnesium sulfate, treated with activated charcoal and then the solvent was distilled off. Thus obtained product was washed with a mixture of diethyl ether and diisopropyl ether and then dried to give 2-(6-formamidopyridin-2-yl)-2-propoxyiminoacetic acid (syn isomer) (1.76 g.), mp 140° to 142° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04267176 |
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| Source dataset | uspto-grants-1981_05 |
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| ORD ID | ord-7d34192ac8124b7398cfd11fc23da36b |
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| Source note | uspto-grants-1981_05 |
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