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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679191Generated: November 2, 2026

Triethylamine → HCID 70620514, compound

https://huagongshe.com/reaction/1679191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 131711054HCID 131711054—
SolventChloroformHCID 6212—
ProductHCID 70620514HCID 70620514103.7%

Reaction Steps

A solution of p-nitrobenzyl 7-azido-6-methoxy-3-acetoxymethyl-ceph-3-em-4-carboxylate (249 mg., 0.54 mMol) in CHCl3 (5 ml.) is cooled in an ice-bath and treated with Et3N (150 μl, 1.08 mMol). H2S is bubbled through the cold solution for 2-3 mins., followed by N2 for 10 mins. The resulting solution is diluted with cold CH2Cl2 (5 ml.), washed with cold dilute HCl to pH 6, cold H2O (3x) and brine, dried with MgSO4, filtered, and evaporated in vacuo to provide a mixture (245 mg.) of p-nitrobenzyl 7β-amino-6α-methoxy-3-acetoxymethyl-ceph-3-em-4-carboxylate and the corresponding 7α-amino-derivative as a yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04079179
Source datasetuspto-grants-1978_03
ORD IDord-a1e4f58af70d4c8e990482d8891ec128
Source noteuspto-grants-1978_03