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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296580Generated: October 30, 2026

Acetone → HCID 70507554, compound

https://huagongshe.com/reaction/2296580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantDiisopropyl EtherHCID 7914—
Reactant7-Aminodeacetoxycephalosporanic acidHCID 33498—
ReactantHCID 20472690HCID 20472690—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductHCID 70507554HCID 70507554—

Reaction Steps

Following a procedure analogous to that of Goldman et al. (loc. cit.), 7-aminodesacetoxycephalosporanic acid (7-amino-3-methylceph-3-em-4-carboxylic acid; 74.9 g., 0.35 mole) is dissolved in well-stirred water (200 ml.) by the slow addition of sodium hydroxide (approximately 75 ml. of 4 N) to a pH of 7.5. To this solution is added 200 ml. of acetone. Keeping the temperature at 10° to 15° C., the isopropyl ether solution of 2-phenyl-2-benzhydryloxycarbonylacetyl chloride prepared above is added with continued strong stirring over 30 minutes. The pH is maintained near 6.5 by the addition of 4 N NaOH (about 160 ml.). Organic solvents are removed by evaporation in vacuo. The aqueous layer is diluted with an equal volume of ethyl acetate and the pH adjusted to 2. The ethyl acetate layer is separated, washed with brine, dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to yield 7-(2-benzhydryloxycarbonyl-2-phenylacetamido)-3-methylceph-3-em-4 -carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04429128
Source datasetuspto-grants-1984_01
ORD IDord-e7620adfc3664b509e3fb8772daa03a5
Source noteuspto-grants-1984_01