HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromocyclopentane → Methyl 3-cyclopentyloxy-4-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromocyclopentane | HCID 8728 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3-hydroxy-4-nitrobenzoate | HCID 294866 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-cyclopentyloxy-4-nitrobenzoate | HCID 21187961 | 102.2% |
Reaction Steps
Cyclopentyl bromide (38.7 g, 0.26 mol) is added slowly (over 1 hour) to a stirred suspension of potassium carbonate (41.4 g, 0.3 mol) in N,N-dimethylformamide (200 mL) containing methyl 3-hydroxy-4-nitrobenzoate (39.4 g, 0.2 tool) at 65° C. and then the stirring is continued for 4 hours. The mixture is allowed to cool and then filtered. The flitrate is diluted with water (700 mL) containing sodium chloride (50 g) and then extracted with toluene (3×200 mL). The combined organic extract is washed with 1N sodium hydroxide solution (1×200 mL) and then water (2×200 mL) and then evaporated under reduced pressure to give methyl 3-cyclopentyloxy-4-nitrobenzoate (54.2 g, 100%) as a pale green solid which is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05698711 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-d3030c42f1554c66ad60990f5658fb82 |
| Source note | uspto-grants-1997_12 |