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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414004Generated: October 26, 2026

Diethyl Ether → Sodium

https://huagongshe.com/reaction/1414004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium 2-ethyl hexanoateHCID 53628222—
Reactant8-Oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, trifluoroacetate saltHCID 77509203—
Solvent1-ButanolHCID 263—
SolventMethanolHCID 887—
ProductSodiumHCID 5360545—
Product8-Oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 19091993—

Reaction Steps

While stirring 0.8 g of [6R-[6α, 7β(Z)]]-3-[(Acetyloxy)methyl]-7-[[(2-amino-4-thiazolyl)[2-oxo-2-[(phenylmethoxy)amino]ethoxy]imino]acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, trifluoroacetate salt is dissolved in 5 ml methanol. At 0° C. an equivalent amount of sodium ethyl hexanoate in butanol is added while stirring. After 10 min. 100 ml of dry diethyl ether is added and the precipitate is filtered off to yield 0.69 g of [6R-[6α, 7β(Z)]]-3-[(Acetyloxy)methyl]-7-[[(2-amino-4-thiazolyl)[2-oxo-2-[(phenylmethoxy)amino]ethoxy]imino]acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, sodium salt having a melting point of 168° C. to 173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04252802
Source datasetuspto-grants-1981_02
ORD IDord-5cc0379f752d49f4993b606a5658b3b7
Source noteuspto-grants-1981_02