HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426817Generated: October 30, 2026
Hydrochloric Acid → HCID 131711642, compound
https://huagongshe.com/reaction/426817
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium 2-ethylbutyrate | HCID 23663635 | — |
| Reactant | HCID 131711636 | HCID 131711636 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 131711642 | HCID 131711642 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04171303 |
|---|
| Source dataset | uspto-grants-1979_10 |
|---|
| ORD ID | ord-0a285c0be7c24dcc81bc85782eb62856 |
|---|
| Source note | uspto-grants-1979_10 |
|---|