HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 4-cyanooxane-4-carboxylate → [4-(Aminomethyl)oxan-4-yl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 4-cyanooxane-4-carboxylate | HCID 16726727 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [4-(Aminomethyl)oxan-4-yl]methanol | HCID 22379474 | — |
Reaction Steps
To the crude product from step 1 (0.944 g, 5.58 mmol) in THF (5 ml) (a dark brown solution) at 0° C. was added LAH (5.58 ml, 5.58 mmol) dropwise via a syringe. The brown mixture was warmed to room temperature and stirred for 18 hours. The resulting mixture was yellow cloudy. LC/MS showed containing desired product. To the reaction was added sodium sulfate decahydrate solid at 0° C. The mixture was stirred at room temperature for 20 min., then filtered and washed with DCM. The yellow filtrate was concentrated in vacuo to give 0.74 g of orange oil. This crude material was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08415381B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-45fcb659298a49e0b6687d8a8cc883d6 |
| Source note | uspto-grants-2013_04 |