HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → 8-(Hydroxymethyl)dibenzo[b,f][1,4]oxazepin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Methyl 11-oxo-10,11-dihydrodibenzo[b,f][1,4]oxazepine-8-carboxylate | HCID 59737222 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-(Hydroxymethyl)dibenzo[b,f][1,4]oxazepin | HCID 86759955 | 46% |
Reaction Steps
Lithium aluminum hydride (11 mL, 11 mmole) was slowly added to the solution of 11-Oxo-10,11-dihydro-dibenzo[b,f][1,4]oxazepine-8-carboxylic acid methyl ester (1.346 g, 5 mmole) in THF under N2 at room temperature. The reaction mixture was stirred for 1 hour and 45 minutes then quenched with 2N of HCl until the pH value reaches 2–3. Removed all the THF by rotary evaporation, and extracted the reaction mixture with ethyl acetate for five times, dried the organic layer with sodium sulfate and filtered and concentrated. Obtained the desired compound (white solid) in 46% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07018997B2 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-aaeb704b2d6b4e9493a13ca513cc7e07 |
| Source note | uspto-grants-2006_03 |