HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentanol → 2-Cyclopentyloxy-4-methoxy-benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentanol | HCID 7298 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Hydroxy-4-methoxybenzonitrile | HCID 11423680 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Cyclopentyloxy-4-methoxy-benzonitrile | HCID 22721165 | 95.9% |
Reaction Steps
To a solution of 2-hydroxy-4-methoxy-benzonitrile (90 mg, 0.60 mmol, example 9), cyclopentanol (55 mg, 0.64 mmol) and triphenylphosphine (167 mg, 0.64 mmol) in THF (3 mL) at −78° C. was added diethyl azodicarboxalate (0.16 mL, 0.860 mmol, 85%). The cooling bath was removed and the reaction was allowed to warm up to room temperature over 1.5 h. The reaction mixture was concentrated in vacuo, and purification of the residue by flash chromatography (Biotage system, KP-Sil™ 32-63 μm, 60 Å silica gel) eluting with 0-8% diethyl ether in hexanes yielded 2-cyclopentyloxy-4-methoxy-benzonitrile as a clear liquid (125 mg, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06734302B2 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-e66ebacc89a543a9934e553575281a43 |
| Source note | uspto-grants-2004_05 |