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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111438Generated: November 3, 2026

Hydrochloric Acid → HCID 13127783, compound

https://huagongshe.com/reaction/1111438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl phosphiteHCID 8472—
ReactantDeacetylcephalothinHCID 93015—
ReactantHCID 178482017HCID 178482017—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
ProductHCID 13127783HCID 13127783118.6%

Reaction Conditions

Temperature22.5 °C

Reaction Steps

To 582 mg of 7β-[2-(2-thienyl)acetamido]-3-hydroxymethyl-3-cephem-4-carboxylic acid and 174 mg of 5-mercapto-1-methyl-1H-tetrazole was added 12 ml of ethyl acetate to make a solution. To the solution were added in sequence 0.25 ml of trimethyl phosphite and 0.2 ml of ether solution of hydrogen chloride (5mol/l), and the mixture was stirred at 20 to 25° C. for 3hours. To the reaction solution was added 10 ml of water, whose pH was adjusted to 2 with 2N HCl, which was then allowed to form two layers. The aqueous layer was taken, to which was added 10 ml of ethyl acetate. The mixture was allowed to form two layers. The organic layers were combined and washed with 5 ml of aqueous saline, which was dried over anhydrous magnesium sulfate, which was then concentrated under reduced pressure. To the concentrate was added ether, then precipitating powdery product was collected by filtration, washed and dried to give 804 mg (yield: 89%) of 3-(1-methyl-1H-tetrazol-5-yl) thiomethyl-7β-[2-(2-thienyl)acetamido]-3-cephem-4-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04980464
Source datasetuspto-grants-1990_12
ORD IDord-f54201e223bb4eb5959c61fe484fc5df
Source noteuspto-grants-1990_12