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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242144Generated: November 3, 2026

Hydrochloric Acid → HCID 21938236, compound

https://huagongshe.com/reaction/1242144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 21938274HCID 21938274—
SolventEthylene GlycolHCID 174—
SolventWaterHCID 962—
ProductHCID 21938236HCID 2193823668.3%

Reaction Conditions

Temperature160 °C

Reaction Steps

2-(2,4-Dichlorobenzoyl)-6-(methoxycarbonyl)-3-methylindole (1.00 g) is suspended in ethylene glycol (10 ml), to which is added hydrazine monohydrate (0.83 g), and stirred under heat at 160° C. for 3 hours. After this is once cooled, potassium hydroxide (1.1 g) is added thereto, and again stirred under heat at 155° C. for 3 hours. After cooled, the reaction mixture is made acidic with water and 1 M HCl added thereto. Then, this is extracted with ethyl acetate. The organic layer is washed with a saturated saline solution, and dried with anhydrous sodium sulfate. Then, the drying agent is removed through filtration, and the filtrate is concentrated under reduced pressure. The resulting crystalline residue is washed with a mixed solution of ethyl acetate and hexane, and dried to obtain 6-carboxy-2-(2,4-dichlorobenzyl)-3-methylindole (86) (0.63 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115647B2
Source datasetuspto-grants-2006_10
ORD IDord-f82cb5884c8d45f6a9b7557c6965adb9
Source noteuspto-grants-2006_10