HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 131711643, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium 2-ethylbutyrate | HCID 23663635 | — |
| Reactant | HCID 131711640 | HCID 131711640 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 131711643 | HCID 131711643 | 85% |
Reaction Steps
A suspension of 48 g. (0.09 moles) of 6-(α-phenoxycarbonyl-phenylacetamido)-2,2-dimethyl-penam-3-carboxylic acid triethylammonium salt in 250 ml. of ethyl acetate is cooled to 0° C., and acidified to pH=2.5 with 2 n aqueous hydrochloric acid. The organic phase is separated, washed with 2×30 ml. of saturated aqueous sodium chloride solution, filtered, and a solution of 12 g. (0.09 moles) of sodium diethylacetate in 50 ml. of acetone is added to the filtrate. The precipitated white powder is filtered off. 36 g. (85%) of 6-(α-phenoxycarbonyl-phenylacetamido)-2,2-dimethyl-penam-3-carboxylic acid sodium salt are obtained; m.p.: 233°-235° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04304717 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-186b008c33e042b0ace9c7883560a7b5 |
| Source note | uspto-grants-1981_12 |