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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480532Generated: October 30, 2026

Pyridine → 2-(Trimethylsilyl)ethyl 2-methylprop-2-enoate

https://huagongshe.com/reaction/480532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethacryloyl chlorideHCID 13528—
Reactant2-(Trimethylsilyl)ethanolHCID 18013—
CatalystPhenothiazineHCID 7108—
SolventDichloromethaneHCID 6344—
Product2-(Trimethylsilyl)ethyl 2-methylprop-2-enoateHCID 2233577744.7%

Reaction Steps

2-Trimethylsilylethanol (Aldrich) (30 g, 0.25 mole) was placed in a round bottom flask equipped with a condenser, addition funnel, magnetic stirrer and a nitrogen inlet. 200 ml dichloromethane, pyridine (20.80 g, 0.26 mole) and 100 mg of phenothiazine were added to the flask. While stirring, methacryloyl chloride (27.18 g, 0.26 mole) in 100 ml dichloromethane was added dropwise at room temperature. A mildly exothermic reaction occurred. The mixture was stirred overnight at room temperature. Afterwards, the mixture was washed with 1×100 ml deionized water and 2×100 ml brine and dried over anhydrous magnesium sulfate. The solution was concentrated in vacuo. Fractional distillation under reduced pressure gave 20.82 grams of the desired product at 35-38° C. at 0.5 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653048B2
Source datasetuspto-grants-2003_11
ORD IDord-5c41783623f34f609e6c00c17305d884
Source noteuspto-grants-2003_11