HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462312Generated: October 30, 2026
Sodium Bicarbonate → HCID 131710998, compound
https://huagongshe.com/reaction/462312
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 21163678 | HCID 21163678 | — |
| Reactant | HCID 21163742 | HCID 21163742 | — |
| Reactant | HCID 131710999 | HCID 131710999 | — |
| Catalyst | Water | HCID 962 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Oxalyl chloride | HCID 65578 | — |
| Product | HCID 131710998 | HCID 131710998 | — |
Reaction Steps
To a cooled (0°-5° C.) suspension of 277 mg. (0.5 mmole) of tert-butyl 7-amino-3-(2'-tert-butoxycarbonylvinyl)-3-cephem-4-carboxylate-p-toluenesulfonate and 420 mg. (5 equivalents) of sodium bicarbonate in 20 cc. of dry acetone there was added about 1 mmole of tert-butyl phenylmalonic acid chloride (prepared from tert-butyl phenyl malonic acid in benzene plus oxalyl chloride and a trace of dimethylformamide [DMF] in acetone). After 10 minutes at 0°-5° C. and one and one-half hours at room temperature, the reaction mixture was re-cooled to 0° C. to 5° C. and a few drops of water was added. After ten minutes this minute was evaporated under reduced pressure to dryness, the residue was taken up in ethyl acetate, the ethyl acetate solution was washed twice with cold 5 percent hydrochloric acid, with saturated aqueous sodium bicarbonate solution, with saturated aqueous sodium chloride solution, and then dried over magnesium sulfate, filtered and evaporated under reduced pressure. The oily tert-butyl 3-(2'-tert-butoxycarbonylvinyl)-7-(2'-tert-butoxycarbonyl-2'-phenylacetamido)-3-cephem-4-carboxylate ester was chromatographed over silica gel 15 percent water and eluted with 2 percent ethyl acetate in benzene. This title ester material crystallized from ethyl ether in the cold, m.p. 168°-170° C. and was characterized by IR, UV [λmax = 317 inμ (ε = 23,000)] and by elemental analysis which follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04065620 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-3e909d16385e478b8da569c3a7cb41f9 |
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| Source note | uspto-grants-1977_12 |
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