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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453411Generated: October 30, 2026

Methyl iodide → HCID 58298857, compound

https://huagongshe.com/reaction/453411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant4-Methoxy-2,3-dimethylbenzoic acidHCID 13440081—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58298857HCID 58298857—

Reaction Conditions

Temperature78 °C

Reaction Steps

2.50 g of 4-methoxy-2,3-dimethylbenzoic acid (G1) are dissolved in 160 ml of tetrahydrofuran under a nitrogen atmosphere and cooled to (−) 78° C. 11.5 ml of sec-BuLi are subsequently added dropwise at such a rate that the temperature of the reaction solution does not exceed (−) 65° C. When the addition is complete, the reddish reaction solution is stirred for a further 30 min with cooling. 3.59 ml of methyl iodide are then slowly added drop-wise. The cooling is subsequently removed, and the mixture is stirred for 1 h. For work-up, 160 ml of water are carefully added. The solution is subsequently extracted twice with 130 ml of ethyl acetate each time. The aqueous phase is cooled in an ice bath with stirring, acidified using 1.0 M HCl and filtered after 30 min. The filter cake is rinsed with cold water and subsequently recrystallised from 2-propanol. The crystals are filtered off with suction and dried for 2 h at 70° C. in vacuo, giving 1.90 g of the title compound as a colourless, crystalline solid having a melting point of 176.7° C.; MS: 194.2 (M+); TLC: Rf=0.29 (diethyl ether/petroleum ether 1:1 parts by volume).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492440B2
Source datasetuspto-grants-2013_07
ORD IDord-d20e21e1a05a4c26b1fbcaff5adfbd33
Source noteuspto-grants-2013_07