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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600132Generated: October 30, 2026

Methyl iodide → 1,2,3,4,5,6,7,8-octapropylanthracene

https://huagongshe.com/reaction/600132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant1,2,3,4,5,6,7,8-octapropyl-9,10-dihydroanthraceneHCID 11432318—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
Product1,2,3,4,5,6,7,8-octapropylanthraceneHCID 1145508998%

Reaction Conditions

Temperature50 °C

Reaction Steps

After 2.2 equivalents of n-BuLi and 2.2 equivalents of tetramethylethylenediamine were added to the hexane solution of 9,10-dihydro-1,2,3,4,5,6,7,8-octapropylanthracene at room temperature, the mixture was heated at 50° C. for 3 hours. The reaction solution was cooled to room temperature and 1.1 equivalent of methyl iodide was added thereto. Stirring for an hour produced the title compound in the NMR yield of 98%. The compound was treated with 3N hydrochloric acid, and washed with saturated sodium hydrogencarbonate aqueous solution and brine. The organic phase was dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to give the pure title compound in the yield of 96%. In this case, purification by column chromatography, etc. was unnecessary.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07901594B2
Source datasetuspto-grants-2011_03
ORD IDord-8d351671d206428789a2c987a1829422
Source noteuspto-grants-2011_03