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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644153Generated: October 26, 2026

2-Methylhexan-2-ol → 2-Methylhexan-2-yl methacrylate

https://huagongshe.com/reaction/1644153

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylhexan-2-olHCID 12240—
ReactantMethacryloyl chlorideHCID 13528—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-Methylhexan-2-yl methacrylateHCID 5447437559%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a flame-dried, nitrogen-purged 500 mL 3-neck roundbottom flask with 250 mL pressure-equalizing addition funnel and magnetic stirbar was charged 81 mL n-butyl lithium (129 mmol, 1 equiv., 1.6 M in hexanes). A degassed solution of 15.0 g 2-methyl-2-hexanol (129 mmol, 1 eq.) in 100 mL anhydrous tetrahydrofuran was charged to the addition funnel and added to the reaction mixture dropwise at 0° C. over 60 minutes. The reaction mixture was warmed for 15 minutes on hot water bath to ensure the reaction was complete. The reaction vessel was cooled to 0° C. and 14.2 g methacryloyl chloride (135 mmol, 1.05 eq.) was added dropwise and allowed to stir for 15 minutes. The addition funnel was replaced with a reflux condenser and the reaction heated to reflux for 20 hours. After the reaction was complete, it was cooled to 0° C. and quenched aqueous sodium bicarbonate. The product was extracted into ethyl ether and the organic phase washed sequentially with aqueous sodium bicarbonate, water, and brine and then dried over magnesium sulfate, filtered, concentrated in vacuo, and stored over a small amount of sodium bicarbonate. The crude product mixture was vacuum distilled through a vacuum-jacketed short-path distillation head to afford 14 g (59%) of 2-methylhexan-2-yl methacrylate (XIII) as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124327B2
Source datasetuspto-grants-2012_02
ORD IDord-2d9feaf84d29429197529d73ba00bfed
Source noteuspto-grants-2012_02