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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390224Generated: November 3, 2026

6-Amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid → HCID 22748504, compound

https://huagongshe.com/reaction/1390224

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acidHCID 162—
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 23335847HCID 23335847—
SolventEthyl AcetateHCID 8857—
ProductHCID 22748504HCID 22748504—

Reaction Steps

Ethoxysulfonyl(2,3-dihydro-5-benzofuranyl)acetic acid (5 mmole) in 50 ml of dry ether is reacted with about 5.5 mmole of thionyl chloride at 20° C. for 4 hours. At the end of this time the solvent is removed to insure that all of the thionyl chloride and hydrochloric acid is removed. It is then redissolved in 10 ml of ether. This ether solution is added to 10 ml of water containing 5 mmole of 6-amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid and 10 mmole of sodium bicarbonate. The temperature of the aqueous solution is about 10° C. After stirring for about 2 hours, the pH is adjusted to about 2. Ethyl acetate is added, the mixture is thoroughly agitated and the layers separated. The organic layer is dried over magnesium sulfate, filtered and evaporated to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04138397
Source datasetuspto-grants-1979_02
ORD IDord-a82fbbc229a04e62909efcc91572dc3d
Source noteuspto-grants-1979_02