HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloro-4-nitrobenzene → 2-Chloro-1-(4-chlorobenzyloxy)-4-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloro-4-nitrobenzene | HCID 7443 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chlorobenzyl alcohol | HCID 13397 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 2-Chloro-1-(4-chlorobenzyloxy)-4-nitrobenzene | HCID 66921922 | 46.9% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
N,N-Dimethylacetamide (42 mL), 16.2 g of 1,2-dichloro-4-nitrobenzene, 12 g of 4-chlorobenzyl alcohol, and 8.7 g of potassium carbonate were mixed together, and the mixture was stirred with heating at 100 to 140° C. for 30 hr. This reaction solution was concentrated under the reduced pressure. The residue was dissolved in 100 mL of ethyl acetate and 100 mL of toluene, and the solution was washed with water and brine. The organic layer was concentrated under the reduced pressure, and the residue was recrystallized from ethanol to give 11.77 g of 2-chloro-1-(4-chlorobenzyloxy)-4-nitrobenzene (yield 46.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07880006B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-8f3e5a6aa3a64f26a10b7bddc406421d |
| Source note | uspto-grants-2011_02 |