HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398157Generated: November 1, 2026
Sodium Nitrite → t-Butyl 3-acetoxymethyl-7beta-[2-hydroxyimino(pyrid-4-yl)acetamido]-ceph-3-em-4-carboxylate
https://huagongshe.com/reaction/2398157
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | t-Butyl 3-acetoxymethyl-7beta-(pyrid-4-ylacetamido)ceph-3-em-4-carboxylate | HCID 131710773 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | t-Butyl 3-acetoxymethyl-7beta-[2-hydroxyimino(pyrid-4-yl)acetamido]-ceph-3-em-4-carboxylate | HCID 137195895 | — |
Reaction Steps
A solution of t-butyl 3-acetoxymethyl-7β-(pyrid-4-ylacetamido)ceph-3-em-4-carboxylate (3.0 g.) in acetic acid (30 ml.) was stirred, cooled briefly in ice and treated dropwise over 3-4 minutes with a solution of sodium nitrite (1.38 g.), in water (10 ml.). The mixture was stirred at 20° for 30 minutes and was then diluted with water and extracted with ethyl acetate. The organic extract was washed with saturated sodium bicarbonate solution and water and then dried over magnesium sulphate. Evaporation almost to dryness gave a residue which was dissolved in the minimum volume of acetone and added dropwise to stirred petroleum spirit (bp. 40°-60°). The resulting solid was collected, washed with petroleum spirit and dried to yield the title oxime as a white powder (2.9 g., 91%) which was shown (NMR) to be a syn-/anti-mixture (30:/0).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04024134 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-de52d507d6ab4ffb99ac25dce598ed4c |
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| Source note | uspto-grants-1977_05 |
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