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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258772Generated: October 29, 2026

Methane → HCID 21426473, compound

https://huagongshe.com/reaction/258772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantSodiumHCID 5360545—
ReactantHCID 21426457HCID 21426457—
ReactantHCID 88826506HCID 88826506—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 21426473HCID 2142647310.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

5-Methoxy-2-thioxo-1,3,4-thiadiazoline (4.43 g.) and sodium bicarbonate (2.27 g.) in water (20 cc.) are added to the sodium salt of 3-acetoxymethyl-2-carboxy-8-oxo-7-[(1,3-dithiol-2-on-4-yl)-acetamido]-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene (12.2 g.) in a buffer (100 cc.) of pH 6.5. The mixture is heated under a nitrogen atmosphere to 50° C., for 5 hours. It is allowed to cool and treated with decolourising charcoal. Ethyl acetate (100 cc.) is added and the mixture is brought to pH 2.5 by adding 5 N hydrochloric acid while stirring. The organic phase is separated off and the aqueous phase is again extracted with ethyl acetate (160 cc.). The combined organic extracts are dried over sodium sulphate, treated with decolourising charcoal and then concentrated to dryness under reduced pressure (20 mm.Hg). A residue (11.5 g.) is obtained, and is triturated with acetonitrile (8 cc.) and isopropyl ether (8 cc.). A solid (2.4 g.) is filtered off and recrystallised from acetonitrile (375 cc.) and isopropyl ether (400 cc.) to give 2-carboxy-3-[(5-methoxy-1,3,4-thiadiazol-2-yl)-thiomethyl]-8-oxo-7-[(1,3-dithiol-2-on-4-yl)-acetamido]-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene (1.52 g.) m.p. 208° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04034090
Source datasetuspto-grants-1977_07
ORD IDord-7faf45f3e3e04b16a7c6e9116fcacb06
Source noteuspto-grants-1977_07