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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679205Generated: October 27, 2026

Diazoethane → HCID 178474225, compound

https://huagongshe.com/reaction/1679205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazoethaneHCID 70695—
ReactantHCID 178475882HCID 178475882—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178474225HCID 178474225—

Reaction Steps

A solution of t-butyl-3-acetoxymethyl-7β-(2-hydroxyiminopyrid-4-ylacetamido)-ceph-3-em-4-carboxylate (syn-isomer) (1.15g) in tetrahydrofuran (20 ml) was treated with an excess of diazoethane at 20° for 40 minutes. The mixture was diluted with ether, washed with water and extracted with 2N-hydrochloric acid. The aqueous extract was neutralized with saturated sodium bicarbonate solution and extracted with ethyl acetate. Evaporation of the dried organic extract offered the title ester as a foam (0.84 g, 69%), [α]D + 47° (c 0.84, DMSO), λmax. (EtOH) 259 nm (ε15,450), νmax. (Nujol) 3300 (NH), 1788 (β-lactam), 1740 (OAc), 1724 (CO2R), 1678 and 1540 cm.-1 (CONH), τ (d6 -DMSO) values include 0.12 (d, J 8Hz; NH), 1.26 and 2.42 (multiplets; aromatic protons), 5.69 (q, J 7Hz, OCH2CH3), 7.93 (s; OCOCH3), 8.50 (s; (CH3)3) and 8.69 (t, J 7Hz; OCH2CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04079178
Source datasetuspto-grants-1978_03
ORD IDord-79b070d3c5e84486ba6fdc5e1d443c7f
Source noteuspto-grants-1978_03