HuagongsheHuagongshe Chemistry Print Report · For research reference only
Borane → 2-(4-Bromo-phenoxy)-propylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Borane | HCID 6331 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-(4-bromophenoxy)propanamide | HCID 2953581 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(4-Bromo-phenoxy)-propylamine | HCID 22388589 | — |
Reaction Steps
A 1M solution of borane in tetrahydrofuran (8.2 ml, 8.2 mmol) was added dropwise to 2-(4-bromo-phenoxy)-propionamide (0.2 g, 0.82 mmol) and the solution was stirred overnight at reflux then subsequently hydrolysed by slow addition of excess of methanol and refluxing for a further 2 hours. The solvent was removed under reduced pressure and aqueous ammonium chloride was added. The aqueous phase was extracted twice with ethyl acetate and the organics were combined, dried over anhydrous magnesium sulfate and concentrated in vacuo to give the desired product. Yield 0.13 g, 68%. LCMS method: 2, RT: 2.74 min; MI: 271-273 [M+1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09012633B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-5b89ec86a6ff46d1b083a9b96345ada4 |
| Source note | uspto-grants-2015_04 |