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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462312Generated: October 30, 2026

Sodium Bicarbonate → HCID 131710998, compound

https://huagongshe.com/reaction/462312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 21163678HCID 21163678—
ReactantHCID 21163742HCID 21163742—
ReactantHCID 131710999HCID 131710999—
CatalystWaterHCID 962—
SolventAcetoneHCID 180—
SolventBenzeneHCID 241—
SolventDimethylformamideHCID 6228—
SolventOxalyl chlorideHCID 65578—
ProductHCID 131710998HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04065620
Source datasetuspto-grants-1977_12
ORD IDord-3e909d16385e478b8da569c3a7cb41f9
Source noteuspto-grants-1977_12