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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182586Generated: October 26, 2026

Triethylamine → Pentadeca-12-ene-1-yl methacrylate

https://huagongshe.com/reaction/2182586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethacryloyl chlorideHCID 13528—
ReactantPentadeca-12-ene-1-olHCID 54287549—
SolventDichloromethaneHCID 6344—
ProductPentadeca-12-ene-1-yl methacrylateHCID 54153362—

Reaction Steps

Pentadeca-12-ene-1-ol (22.6 grams) is placed in a three-neck flask under a blanket of nitrogen. The entire reaction contents are cooled in an ice bath. Methacryloyl chloride (10.5 grams) dissolved in about 50 mL of methylene chloride is added slowly to the cooled pentadeca-12-ene-1-ol with vigorous stirring in about 2 hours. Triethylarnine (11.5 g) dissolved in 25 mL of methylene chloride is subsequently added in about an hour. After addition of triethylamine, the solution is allowed to warm to ambient temperature and is stirred for another 4 hours in order to complete the reaction. The precipitated triethylammonium chloride is removed by filtration, and the filtrate is washed with brine solution (saturated NaCl) followed by washings with dil. NaOH and dil. HCl. The organic layer is dried with anhydrous magnesium sulfate and the solvent is removed in vacuo to yield pentadeca-12-ene-1-yl methacrylate in good yields. Pentadeca-12-ene-1-yl methacrylate is stabilized from polymerization by addition of approximately 10 ppm hydroquinone. The structure of the product is verified by 1H and 13C NMR spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897255B1
Source datasetuspto-grants-2005_05
ORD IDord-2695b4f346074c82bac0d04076303e5b
Source noteuspto-grants-2005_05