Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 67790551 | HCID 67790551 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86743480 | HCID 86743480 | — |
Reaction Steps
To an anhydrous THF solution (3 ml) of LDA, as produced from diisopropylamine (0.03 ml, 0.19 mmol) and a 15% n-butyllithium hexane solution (0.12 ml, 0.19 mmol), anhydrous THF solution (2 ml) of the carbapenam (VI) (16 mg, 0.08 mmol) was added dropwise at -78° C. under a carbapenam (VI) (16 mg, 0.08 mmol) was added dropwise at -78° C. under a current of argon. The mixture was stirred for 30 minutes and a mixture of acetic acid and methanol (1:1, v/v) (0.5 ml) was added. It was warmed to room temperature and extracted with ether. The ether layer was washed with water and dried with anhydrous magnesium sulfate. The solvent was distilled off and the thus obtained residue was subjected to HPLC purification. A fraction eluting with a mixture of n-hexane and ethyl acetate (9:1, v/v) gave a mixture (12 mg) of a carbapenam in the 5,6-cis form (IX) with a small quantity of by-product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05118831 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-1cdba9fe42024fc0b457f2e776311eeb |
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| Source note | uspto-grants-1992_06 |
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