HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31342Generated: October 23, 2026
Diethyl Ether → 5-Chloro-3-hydroxy-3-(2-methoxyphenyl)indolin-2-one
https://huagongshe.com/en/reaction/31342
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-Bromoanisole | HCID 11358 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-chloro-1H-indole-2,3-dione | HCID 87203 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Chloro-3-hydroxy-3-(2-methoxyphenyl)indolin-2-one | HCID 21905955 | — |
| Product | HCID 178489560 | HCID 178489560 | — |
Reaction Steps
This compound is prepared according to the procedure disclosed in WO 95/18105. A solution of 2-methoxyphenylmagnesium bromide is prepared from 16 g of magnesium in 35 ml of ether and from a solution of 124 g of 1-bromo-2-methoxybenzene in 175 ml of ether. This solution is added dropwise under an argon atmosphere to a mixture, cooled beforehand in an ice bath, of 30 g of 5-chloro-1H-indole-2,3-dione in 250 ml of THF and then the mixture is left stirring while allowing the temperature to rise to RT. After stirring for 1 hour at RT, the reaction mixture is slowly poured into saturated NH4Cl solution and the THF is evaporated off under vacuum. The precipitate formed is spin-filtered off and is washed with iso ether. 42 g of the expected product are obtained, which product is used without further purification in the following stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07425566B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-63ed12e504da457c9655396a881f37c0 |
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| Source note | uspto-grants-2008_09 |
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