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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224791Generated: October 25, 2026

Hydrochloric Acid → 6,6-Dibromopenicillanic acid sulfone

https://huagongshe.com/reaction/224791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhosphoric AcidHCID 1004—
ReactantSodium ChlorideHCID 5234—
ReactantSodium HydroxideHCID 14798—
ReactantPermanganateHCID 24401—
Reactant6,6-Dibromopenicillanic acidHCID 90376—
ReactantPotassium PermanganateHCID 516875—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product6,6-Dibromopenicillanic acid sulfoneHCID 1427720—

Reaction Steps

To the dichloromethane solution of 6,6-dibromopenicillanic acid from Preparation J was added 300 ml. of water, followed by the dropwise addition over a period of 30 minutes of 3N sodium hydroxide. The pH stabilized at 7.0. The aqueous layer was removed and the organic layer was extracted with water (2×100 ml.). To the combined aqueous solutions was added, at -5° C., a premixed solution prepared from 59.25 g. of potassium permanganate, 18 ml. of concentrated phosphoric acid and 600 ml. of water, until the pink color of the permanganate persisted. The addition took 50 minutes and 550 ml. of oxidant were required. At this point 500 ml. of ethyl acetate was added and then the pH was lowered to 1.23 by the addition of 105 ml. of 6N hydrochloric acid. Then 250 ml. of 1M sodium bisulfite was added during 10-15 minutes at ca. 10° C. During the addition of the sodium bisulfite solution the pH was maintained at 1.25-1.35 using 6N hydrochloric acid. The aqueous phase was saturated with sodium chloride and the two phases were separated. The aqueous solution was extracted with additional ethyl acetate (2×150 ml.) and the combined ethyl acetate solutions were washed with brine and dried (MgSO4). This afforded an ethyl acetate solution of 6,6-dibromopenicillanic acid 1,1-dioxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04234579
Source datasetuspto-grants-1980_11
ORD IDord-b4dfba880741421f93d57bc84cc848cc
Source noteuspto-grants-1980_11