HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1-(Allyloxy)-2-chloro-5-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-5-nitrophenol | HCID 69264 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(Allyloxy)-2-chloro-5-nitrobenzene | HCID 12881930 | — |
Reaction Steps
A mixture of 7.4 g of 2-chloro-5-nitrophenol, 5.4 g of allyl bromide, 5.9 g of anhydrous potassium carbonate and 50 mL of dry N,N-dimethylformamide (DMF) was stirred at room temperature over a weekend. Then the mixture was poured into water, and the resulting mixture was extracted twice with ethyl acetate and twice with ether. The combined extracts were washed with water, then with brine, dried (Na2SO4), filtered and stripped of the solvents. The residue was recrystallized from hexane to give 1-(allyloxy)-2-chloro-5-nitrobenzene (3A), as orange needles, m.p.: 58°-59.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04881967 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-f816798a8c764ad9be95c840296571e5 |
| Source note | uspto-grants-1989_11 |