HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Methyl 2-[2-[4-(3-chloro-4,5,6,7-tetrahydroindazol-2-yl)-3-fluorophenoxymethyl]-5-chlorophenoxy]propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-2-(2-fluoro-4-hydroxyphenyl)-4,5,6,7-tetrahydroindazole | HCID 18981048 | — |
| Reactant | Methyl 2-(2-chloromethyl-5-chlorophenoxy)propionate | HCID 53768369 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-[2-[4-(3-chloro-4,5,6,7-tetrahydroindazol-2-yl)-3-fluorophenoxymethyl]-5-chlorophenoxy]propionate | HCID 18981019 | 81.1% |
Reaction Steps
By the method of Example 1, Step K, 0.49 g (0.0016 mole) of 3-chloro-2-(2-fluoro-4-hydroxyphenyl)-4,5,6,7-tetrahydroindazole and 0.52 g (0.002 mole) of methyl 2-(2-chloromethyl-5-chlorophenoxy)propionate (Example 2, Step F) were reacted in the presence of 0.41 g (0.003 mole) of anhydrous potassium carbonate in 30 mL of N,N-dimethylformamide, yielding 0.64 g of methyl 2-[2-[4-(3-chloro-4,5,6,7-tetrahydroindazol-2-yl)-3-fluorophenoxymethyl]-5-chlorophenoxy]propionate as a syrup. The NMR and IR spectra were consistent with the proposed structure. NMR: 1.64 (d, 3H, JHH =8.0 Hz); 1.82 (m, 4H); 2.50 (t, 2H, JHH =4.0 Hz); 2.68 (t, 2H, JHH =4.0 Hz); 3.76 (s, 3H); 4.82 (q, 1H, JHH =8 Hz); 5.18 (s, 2H,); 6.78-7.40 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05262390 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-92676696a6ef4a8baf3f07cc442826f0 |
| Source note | uspto-grants-1993_11 |