HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Sodium Tartrate → HCID 57833588, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Sodium Tartrate | HCID 9357 | — |
| Reactant | HCID 15986284 | HCID 15986284 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57833588 | HCID 57833588 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of 9-[8-(2,2,2-trifluoroacetyl)-8-aza-bicyclo[3.2.1]oct-3-ylidene]-9H-xanthene-4-carboxylic acid methyl ester in methylene chloride (0.001 to 1 M solution) at −78° C. may be treated with diisobutyl aluminum hydride (1M in cyclohexane; 2 to 10 equiv), and the mixture may be allowed to slowly warm up to 0° C. After stirring at that temperature for a period of 1 to 5 hr, an aqueous solution of Rochelle's salt may be added. The mixture may be extracted with an appropriate organic solvent such as ethyl acetate, and the organic layer may be dried over a suitable drying agent such as potassium carbonate. After filtration and evaporation, the residue may be purified via reverse phase column chromatography to yield Compound 2e.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07582650B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-a747c5c83e864d11bd6c0f1a7ec166df |
| Source note | uspto-grants-2009_09 |