HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593396Generated: October 23, 2026
2-Bromoanisole → 3-Hydroxy-3-(2-methoxyphenyl)-5-trifluoromethoxy-1,3-dihydro-2H-indol-2-one
https://huagongshe.com/en/reaction/1593396
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromoanisole | HCID 11358 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-(trifluoromethoxy)-2,3-dihydro-1H-indole-2,3-dione | HCID 2732752 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Hydroxy-3-(2-methoxyphenyl)-5-trifluoromethoxy-1,3-dihydro-2H-indol-2-one | HCID 21905899 | 76.3% |
| Product | HCID 178489560 | HCID 178489560 | — |
Reaction Steps
A solution of 2-methoxyphenylmagnesium bromide is prepared from 1.9 g of magnesium in 4 ml of ether and from a solution of 14.54 g of 1-bromo-2-methoxybenzene in 21 ml of ether. This solution is added drop wise, under an argon atmosphere, to a mixture of 5 g of 5-trifluoromethoxy-1H-indole-2,3-dione in 26 ml of THF, cooled beforehand in an ice bath, and then heated at the reflux point of the ether for 1 hour 30 minutes and allowed to cool to RT. The reaction mixture is poured slowly into saturated NH4Cl solution and extracted with EtOAc, the organic phase is washed with 5% K2CO3 solution, with water and with saturated NaCl solution and dried over Na2SO4, and the solvent is evaporated off under vacuum. 2.8 g of the expected product are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07297692B2 |
|---|
| Source dataset | uspto-grants-2007_11 |
|---|
| ORD ID | ord-3564bb8751494add800b81fcea59bebe |
|---|
| Source note | uspto-grants-2007_11 |
|---|