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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051069Generated: October 29, 2026

Methyl Acrylate → HCID 19784863, compound

https://huagongshe.com/reaction/2051069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantHCID 9838139HCID 9838139—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19784863HCID 1978486348.9%

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of 20.0 grams (76 mmol) of 4-benzyloxyl-oxyl-2,2,6,6-tetramethylpiperidine, 10.0 grams of anhydrous magnesium sulfate, 500 mg of 5% palladium on carbon and 150 ml of tetrahydrofuran is hydrogenated on a Parr apparatus (50 psi, ambient temperature). Catalyst and drying agent are removed by filtration and the filtrate is quickly transferred to a flask under a nitrogen atmosphere. To the flask are added 0.85 gram of potassium tert-butoxide, 19.7 grams (229 mmol) of methyl acrylate, and 50 ml of tetrahydrofuran. The reaction mixture is stirred at ambient temperature for three hours and at 55° C. for one hour. The reaction mixture is partitioned between ether (300 ml) and saturated sodium bicarbonate solution (150 ml). The ether layer is washed with water (2×500 ml), washed with saturated aqueous sodium chloride (200 ml), dried over anhydrous magnesium sulfate and concentrated to an oil. The oil is purified by flash chromatography (silica gel; 9:1 hexane:ethyl acetate) to afford 13.0 grams of the title compound as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05015678
Source datasetuspto-grants-1991_05
ORD IDord-87803e8794af44caa0b9099434a386fd
Source noteuspto-grants-1991_05