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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248614Generated: October 30, 2026

Methyl iodide → HCID 20277052, compound

https://huagongshe.com/reaction/1248614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantIodide IonHCID 30165—
ReactantHCID 20277050HCID 20277050—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
ProductHCID 20277052HCID 20277052—

Reaction Steps

6-Fluoro-3-(4'-fluorophenyl)-1-hydroxy-1-pyrid-4-ylindane (5.0 g) was reacted with methyliodide as described in Example 2, and the resulting pyridylium iodide (viscous oil) was dissolved in ethanol (150 ml) and 0.5 g PtO2 added. The estimated amount of hydrogen was consumed in 3 hrs. (3.0-3.5 atm.). The catalyst was filtered off and the ethanol evaporated. Ice-cold NaOH solution (100 ml 0.2M) was added to the residue and the resulting base extracted with ethyl acetate (2×50 ml). The combined organic phases were dried (MgSO4) and the solvent evaporated. The remaining oil was dissolved in isopropylether, and by cooling the product precipitated and was filtered off. Yield: 4.7 g (88.8%) of the title compound. MP: 146°-147° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04525360
Source datasetuspto-grants-1985_06
ORD IDord-1b73a2a7dd9a4bcab05e71cf0bf59594
Source noteuspto-grants-1985_06