HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952368Generated: November 3, 2026
Potassium Hydroxide → HCID 59529753, compound
https://huagongshe.com/reaction/1952368
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 86646329 | HCID 86646329 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 59529753 | HCID 59529753 | — |
Reaction Steps
2-chloro-3-(3,5-dibromophenoxy)-4-(trifluoromethyl)-1,2-dihydropyridine (1.64 g, 3.80 mmol) and potassium hydroxide (0.640 g, 11.4 mmol) were dissolved in tert-butanol in a round bottom flask and placed in an oil bath at 75° C. under N2. After 16 hours, the reaction mixture was allowed to cool to room temperature and quenched with saturated aqueous ammonium chloride (25 mL). This mixture was diluted with water (25 mL) and extracted with ethyl acetate (2×50 mL). The combined organic extracts were washed with brine (2×50 mL), dried (MgSO4), filtered and the solvent was evaporated under reduced pressure to give the title compound as a white solid. 1H NMR (DMSO-d6) δ 12.68 (s, 1H), 7.58 (d, J=6.8 Hz, 1H), 7.54-7.52 (m, 1H), 7.24-7.22 (m, 2H), 6.47 (d, J=Hz, 1H). LRMS (M+1)=413.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08404856B2 |
|---|
| Source dataset | uspto-grants-2013_03 |
|---|
| ORD ID | ord-5e1f239da67b4f349083b085f69a4932 |
|---|
| Source note | uspto-grants-2013_03 |
|---|