HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → [4-(Aminomethyl)phenyl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(Aminomethyl)Benzoic Acid | HCID 65526 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Oxolane--water (1/1) | HCID 21881883 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [4-(Aminomethyl)phenyl]methanol | HCID 6496943 | 38.7% |
Reaction Steps
A! 4-(Aminomethyl)benzoic acid (20 g, 0.132 mole) was added to a suspension of lithium aluminium hydride (5.5 g, 0,145 moles) in 300 ml of THF, at room temperature. The suspension was refluxed for 4 hours, the cooled to room temperature and added with, successively, a mixture THF/water 7:1 (32 ml), 32% sodium hydroxide (10 ml) and water (40 ml). The formed solid was filtered off and the solvent evaporated under vacuum to provide 7 g of 4-(aminomethyl)benzyl alcohol che was directly used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05827881 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-ae771e1a25344d29a48a161ce5ddfaab |
| Source note | uspto-grants-1998_10 |