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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580716Generated: November 4, 2026

4-Iodoanisole → HCID 21563763, compound

https://huagongshe.com/reaction/1580716

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodoanisoleHCID 69676—
ReactantHCID 21543496HCID 21543496—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductHCID 21563763HCID 21563763—

Reaction Steps

5.6 G (0.02 mole) of 1-(4-methoxyphenyl)-3-(2-oxopropyl)indole, prepared as described in example 1 but using 4-methoxyiodobenzene instead of iodobenzene are dissolved in 50 ml of anhydrous ethanol in a 200 ml autoclave. 2 g of Raney nickel are added. The autoclave is brought to a pressure of 50 kg of hydrogen and heat is applied at 100° for 8 hours at this pressure. The reaction medium is taken to dryness and the residue dissolved in normal acetic acid in the presence of diethyl ether. The organic phase is dried and the solvents are removed. The residue is then distilled.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03933853
Source datasetuspto-grants-1976_01
ORD IDord-420b040125554748a341356be1b92f7d
Source noteuspto-grants-1976_01