HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 131716592, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Tetrabutylammonium Fluoride Trihydrate | HCID 11726816 | — |
| Reactant | HCID 131716592 | HCID 131716592 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70398597 | HCID 70398597 | 6% |
| Product | HCID 131716592 | HCID 131716592 | 27.1% |
Reaction Steps
This product (b) (2.1 g; 3.69 millimoles) is dissolved in tetrahydrofuran (10 ml), mixed with acetic acid (0.8 ml) and tetrabutylammonium fluoride trihydrate (2.78 g; 2.4 equivalents) and kept at room temperature for two nights as in Example B'-12 to give 6α-(1-hydroxyethyl)-1-methyl-2-(4-pyridylthio)methylidene-1-carbapenam-3-carboxylic acid p-methoxybenzyl ester (100 mg; Yield: 6.0%, from less polar fraction) and 6α-(1-hydroxyethyl)-1-methyl-2-(4-pyridylthio)methyl-1-carbapen-2-em-3-carboxylic acid p-methoxybenzyl ester (b) (455 mg; Yield: 27.1%; having physical constants as follows from polar fraction).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04960879 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-17d374e50a164247a5aaeb1d2406ce93 |
| Source note | uspto-grants-1990_10 |