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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646402Generated: October 30, 2026

Phenylhydrazine → 3H-Indole, 2,3,3-trimethyl-

https://huagongshe.com/reaction/1646402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazineHCID 7516—
Reactant3-Methyl-2-butanoneHCID 11251—
ReactantSodium BisulfateHCID 516919—
SolventWaterHCID 962—
Product3H-Indole, 2,3,3-trimethyl-HCID 1542797.5%

Reaction Steps

226 g (2 mol) of phenylhy-drazine (95.7% pure) were initially introduced at 90° C. in a solution of 5 mol of sodium hydrogen sulphate in 1900 ml of water. 225 ml (2.1 mol) of methyl isopropyl ketone were added dropwise in the course of 30 min. The mixture was stirred for 3 h at 90° to 100° C. After cooling, the batch was neutralised and the organic phase was separated off and distilled. 299.3 g of 97.5% pure 2,3,3-trimethylindolenine were obtained Yield: 91.6% of the theoretical yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05179211
Source datasetuspto-grants-1993_01
ORD IDord-7cbbfff0c62b4ca99801784b33c152f2
Source noteuspto-grants-1993_01