HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromocyclopentane → Methyl 3-(cyclopentyloxy)-4-methoxy-2-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromocyclopentane | HCID 8728 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3-hydroxy-4-methoxy-2-nitrobenzoate | HCID 59268115 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 3-(cyclopentyloxy)-4-methoxy-2-nitrobenzoate | HCID 66781723 | — |
Reaction Steps
A mixture of methyl 3-hydroxy-4-methoxy-2-nitrobenzoate (1.14 g, 5.0 mmol), bromocyclopentane (0.7 mL, 6.5 mmol), potassium carbonate (2.0 g, 14 mmol), and anhydrous acetonitrile (15 mL) was refluxed under N2. After 19 h, the reaction was allowed to cool to rt, concentrated, and purified by silica gel chromatography (4:1→3:2; hexanes:ethyl acetate) to give methyl 3-(cyclopentyloxy)-4-methoxy-2-nitrobenzoate: MS (ESI): 296.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08080563B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-8201c766f1c3470e9d7ab512b5e95e41 |
| Source note | uspto-grants-2011_12 |