HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 44217645, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 66846925 | HCID 66846925 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 44217645 | HCID 44217645 | 104.4% |
Reaction Steps
To a solution of benzyl 1-benzyl-5-methoxy-1H-indazole-3-carboxylate (17.7 g; 0.05 mol), diethyl ether (100 ml) and tetrahydrofuran (THF) (170 ml) stirred at room temperature was slowly added LiAlH4 (3.8 g; 0.1 mol). Once the addition was complete, the suspension was stirred at reflux for 24 hours. The reaction was stopped by destroying the excess LiAlH4 via addition of water (40 ml) and 5N NaOH (10 ml). The organic phase was separated out and the solvent was evaporated off under reduced pressure. The crude residue obtained was purified by crystallization from 95° ethanol to give 14 g of (1-benzyl-5-methoxy-1H-indazol-3-yl)methanol with a melting point of 97-98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08835481B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-57b977404ba44b888fdb882aedf74dfd |
| Source note | uspto-grants-2014_09 |