HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187880Generated: November 1, 2026
1-(Azidomethyl)-3-(phenylmethoxy)benzene → (3-(Benzyloxy)phenyl)methanamine
https://huagongshe.com/reaction/2187880
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(Azidomethyl)-3-(phenylmethoxy)benzene | HCID 11806729 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-(Benzyloxy)phenyl)methanamine | HCID 11009288 | — |
Reaction Steps
3-Benzyloxybenzyl azide, as described above in Step A, (5.0 g, 20.9 mmol) was dissolved in dry THF (100 mL) and the solution was cooled to −70° C. Lithium aluminum hydride (31.4 mL of a 1.0 M solution in THF, 31.4 mmol) was added dropwise, then the reaction mixture was warmed to 0° C. and stirred for 30 min. The reaction was quenched with EtOAc (1.2 mL), then water (1.2 mL), then 15% NaOH (1.2 mL), and finally water (3.6 mL). The resulting mixture was filtered, concentrated under reduced pressure and purified by flash column chromatography on silica, eluting with CH2Cl2-3% MeOH −0.3% NH40H, to yield the titled product as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06410534B1 |
|---|
| Source dataset | uspto-grants-2002_06 |
|---|
| ORD ID | ord-a9fd0702b0954673b294e6df05235f40 |
|---|
| Source note | uspto-grants-2002_06 |
|---|