HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064580Generated: October 29, 2026
Aluminium lithium hydride → HCID 22477758, compound
https://huagongshe.com/reaction/2064580
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 22478065 | HCID 22478065 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22477758 | HCID 22477758 | 67.4% |
Reaction Steps
11.1 mg of lithium aluminium hydride are added to a solution of 76 mg of methyl 2-benzyl-5-ethoxy-2H-pyrazole-3-carboxylate in 0.75 ml of tetrahydrofuran, cooled to a temperature in the region of 0° C. by an ice bath. After 3 hours at a temperature in the region of 0° C., 22.2 mg of lithium aluminium hydride are added and the reaction medium is allowed to warm to a temperature in the region of 20° C. After 30 minutes at a temperature in the region of 20° C., 10 ml of ice-cold water are added and the reaction mixture is then filtered through Celite. After separation of the phases by settling, the aqueous phase is extracted with ethyl acetate. The organic phases are combined, dried over magnesium sulphate and concentrated under reduced pressure. 45.7 mg of (2-benzyl-5-ethoxy-2H-pyrazol-3-yl)methanol are thus obtained in the form of a brown lacquer, the characteristics of which are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08288425B2 |
|---|
| Source dataset | uspto-grants-2012_10 |
|---|
| ORD ID | ord-2523b517b5924a78a6166f39d1d30a9f |
|---|
| Source note | uspto-grants-2012_10 |
|---|