HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → N-(1-benzyl-4-piperidinyl)-2-hydroxymethyl-3-fluoroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 2-(1-Benzyl-4-piperidinylamino)-6-fluorobenzoic acid | HCID 54016753 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(1-benzyl-4-piperidinyl)-2-hydroxymethyl-3-fluoroaniline | HCID 19031041 | 60.1% |
Reaction Steps
To a solution of lithium aluminium hydride (0.9 g) in anhydrous tetrahydrofuran (160 ml) is added 2-(1-benzyl-4-piperidinylamino)-6-fluorobenzoic acid (8.0 g) and the mixture is refluxed for 1 hour. After cooling, the reaction solution is poured into ice-water and then extracted with dichloromethane. The solvent is concentrated and to the resulting residue is added diethyl ether/n-hexane. The precipitated crystal is collected by filtration to give N-(1-benzyl-4-piperidinyl)-2-hydroxymethyl-3-fluoroaniline (4.6 g) as light yellow powders, m.p.: 167°-170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05225402 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-a90139276623445080cfa5a03b2a7c6d |
| Source note | uspto-grants-1993_07 |