HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium sodium tartarate → [1-(2,6-Dichlorobenzyl)-1H-imidazol-5-yl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl 1-(2,6-dichlorobenzyl)-1H-imidazol-5-carboxylate | HCID 67407845 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | [1-(2,6-Dichlorobenzyl)-1H-imidazol-5-yl]methanol | HCID 67409440 | — |
Reaction Steps
220 mg (0.74 mmol) of the compound from Example 32A were dissolved in 3 ml of THF, and 0.74 ml (0.74 mmol) of a 1 M solution of lithium aluminum hydride in THF was added dropwise at 0° C. The mixture was stirred at RT for 1 h. For work-up, 5 ml of a saturated potassium sodium tartrate solution were added with ice cooling, the mixture was diluted with 10 ml of ethyl acetate and the precipitated solid was filtered off. The crude product was purified chromatographically [Method 19]. This gave 188 mg (99% of theory) of the target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187466B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-2e65ef34618443cc8a71a38ec0be8312 |
| Source note | uspto-grants-2015_11 |