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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid | HCID 162 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 23335847 | HCID 23335847 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22748504 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04138397 |
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| Source dataset | uspto-grants-1979_02 |
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| ORD ID | ord-a82fbbc229a04e62909efcc91572dc3d |
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| Source note | uspto-grants-1979_02 |
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