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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965533Generated: October 30, 2026

Ammonium Chloride → 5-Chloro-3-(cyclohexylmethyl)-1,3-dihydro-3-hydroxyindol-2-one

https://huagongshe.com/reaction/965533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant5-chloro-1H-indole-2,3-dioneHCID 87203—
ReactantCyclohexane, (bromomethyl)-HCID 137636—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-3-(cyclohexylmethyl)-1,3-dihydro-3-hydroxyindol-2-oneHCID 19076380—
ProductHCID 178419664HCID 178419664—

Reaction Steps

A solution of cyclohexylmethylmagnesium bromide is prepared from 5.37 g of magnesium and 30.8 ml of bromomethylcyclohexane in 15 ml of ether. This solution is added dropwise at +4° C., under an argon atmosphere, to a mixture of 10 g of 5-chloroisatin and 25 ml of THF. After stirring for 3 hours at RT, 500 ml of a saturated solution of ammonium chloride are added, extraction is carried out with AcOEt, the organic phase is washed with a saturated solution of NaCl and with water and dried over sodium sulfate and the solvent is evaporated off under vacuum to give 12 g of the expected product after crystallization from AcOEt and recrystallization from a THF/AcOEt mixture. M.p.=252°-253° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05773612
Source datasetuspto-grants-1998_06
ORD IDord-45faaedb2c7e44e8baf3c25a35b350c9
Source noteuspto-grants-1998_06