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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium NitriteHCID 23668193—
Reactantt-Butyl 3-acetoxymethyl-7beta-(pyrid-4-ylacetamido)ceph-3-em-4-carboxylateHCID 131710773—
SolventAcetic AcidHCID 176—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Productt-Butyl 3-acetoxymethyl-7beta-[2-hydroxyimino(pyrid-4-yl)acetamido]-ceph-3-em-4-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04024134
Source datasetuspto-grants-1977_05
ORD IDord-de52d507d6ab4ffb99ac25dce598ed4c
Source noteuspto-grants-1977_05