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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426817Generated: October 30, 2026

Hydrochloric Acid → HCID 131711642, compound

https://huagongshe.com/reaction/426817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantSodium 2-ethylbutyrateHCID 23663635—
ReactantHCID 131711636HCID 131711636—
SolventAcetoneHCID 180—
ProductHCID 131711642HCID 13171164280%

Reaction Steps

A suspension of 25 g. (0.048 moles) of 6-(α-[5-indanyloxycarbonyl]-phenylacetamido)-2,2-dimethyl-penam-3-carboxylic acid triethylammonium salt in 150 ml. of ethyl acetate is cooled to 0° C., and the suspension is acidified with 2 n aqueous hydrochloric acid (18 ml.) to pH=2. The organic phase is separated and the aqueous-acidic phase is extracted with 2×20 ml. of ethyl acetate. The organic solutions are combined, washed with 3×30 ml. of saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered, and neutralized with a solution of 6.7 g. (0.048 moles) of sodium diethylacetate in 30 ml. of acetone. About 50% of the solvent is evaporated in vacuo. 100 ml. of diisopropyl ether are added to the concentrate, the mixture is cooled, and the obtained white, powdery substance is filtered off. 18 g. (80%) of 6-(α-[5-indanyloxycarbonyl]-phenylacetamido)-2,2-dimethyl-penam-3-carboxylic acid sodium salt are obtained; m.p.:b 220°-222° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04171303
Source datasetuspto-grants-1979_10
ORD IDord-0a285c0be7c24dcc81bc85782eb62856
Source noteuspto-grants-1979_10