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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482827Generated: October 30, 2026

Sulfuric Acid → HCID 70456312, compound

https://huagongshe.com/reaction/482827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium PermanganateHCID 516875—
ReactantMonobasic potassium phosphateHCID 516951—
ReactantSodium PyrosulfiteHCID 656671—
ReactantHCID 13619047HCID 13619047—
SolventWaterHCID 962—
ProductHCID 70456312HCID 704563126%

Reaction Conditions

Temperature15 °C

Reaction Steps

The crude 3-ethyl-4-[2-(hydroxy)ethyl]-2-azetidinone (34 g; 0.237 mol) obtained according to step (c) is added to 63 g (0.394 mol) of potassium permanganate and 79 g (0.59 mol) of potassium dihydrogen phosphate in 870 ml of water. The mixture is maintained under stirring at 15° C. for 22 hours, then 220 ml of a saturated solution of sodium metabisulfite are added thereto maintaining the value of the pH at about 3 by the gradual addition of 220 ml of 10% sulfuric acid. The mixture is stirred under cooling at 5° C. until a clear solution is obtained (about 30 minutes), then, after saturation with ammonium sulfate, it is extracted with four 250-ml portions of ethyl acetate. The organic extracts are pooled together and dried over MgSO4. Concentration of the ethyl acetate solution to 100 ml and cooling overnight in a refrigerator gives a crystalline precipitate which is recovered by filtration. Yield 16.43 g of the product of the title. Concentration of the mother liquors yields 2.23 g of the product. Elemental analysis, I.R. and N.M.R. data are in agreement with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04576746
Source datasetuspto-grants-1986_03
ORD IDord-9f59222617074e70b0174cb36d0132a3
Source noteuspto-grants-1986_03