HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-Chloro-2-fluoro-5-(2,2-difluorocyclopropylmethoxy)nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenol, 2-chloro-4-fluoro-5-nitro- | HCID 158655 | — |
| Reactant | 2-(Bromomethyl)-1,1-difluorocyclopropane | HCID 2761402 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Chloro-2-fluoro-5-(2,2-difluorocyclopropylmethoxy)nitrobenzene | HCID 14129431 | — |
Reaction Steps
3.6 g 2-Chloro-4-fluoro-5-nitrophenol was dissolved in dimethylformamide and treated with potassium carbonate. The mixture was stirred at room temperature for one hour and then 3.3 g 2,2-difluorocyclopropylmethyl bromide added. It was the heated at 80° C. for 2 hours and added to water. The mixture was extracted with methylene chloride and the organic phase washed with saturated brine, dried over magnesium sulphate and concentrated. The residue was chromatographed on silica gel using a mixture of 3 parts hexane and 1 part ethyl acetate. There was obtained 5 g (=93% of theory) of yellow crystals whose nmr spectrum is as follows: δ=1.1-2.4 ppm (m) 3H, δ=4.15 ppm (d 7 Hz,tr 1.5 Hz) 2H, δ=7.35 ppm (d 10 Hz) 1H, δ=7.5 ppm (d 7 Hz) 1H.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04859230 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-0f2e047be0434378acb8cf00e7bd41a0 |
| Source note | uspto-grants-1989_08 |