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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1598410Erstellt: 27. Oktober 2026

Triethylamine → N-(Acryloyloxyethoxyethyl)hexahydrophthalimide

https://huagongshe.com/reaction/1598410

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktAcryloyl chlorideHCID 13140—
EduktN-(2-hydroxyethoxyethyl)hexahydrophthalimideHCID 55023972—
KatalysatorPhenothiazineHCID 7108—
LösungsmittelAcetoneHCID 180—
ProduktN-(Acryloyloxyethoxyethyl)hexahydrophthalimideHCID 6762210959,5%

Reaktionsschritte

A one liter, three necked flask was equipped with overhead stirrer, nitrogen atmosphere and an addition funnel. The flask was charged with 100 g of N-(2-hydroxyethoxyethyl)hexahydrophthalimide (0.41 mol.), 42 g of triethylamine (0.41 mol.), 1 g of phenothiazine and 400 ml of acetone. Next, 38 g of acryloyl chloride (0.41 mol.) was added slowly to the flask via the addition funnel over 45 minutes. The reaction was stirred for an additional 12 hours. The triethylamine hydrochloride salt was removed by filtration and the remaining mother liquor was evaporated with a rotoevaporator. The resulting red-orange liquid was dissolved in chloroform and extracted with HCl(10%), NaCl(aq.), NH4OH(10%), NaCl(aq.) and dried over MgSO4. The chloroform was removed with a rotoevaporator to yield 72 g (59%) of an orange-red liquid. The product was confirmed by IR and 13C NMR.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05736747
Quelldatensatzuspto-grants-1998_04
ORD IDord-a11f5bb7c80d4f25a74dbe7f62a23293
Quellennotizuspto-grants-1998_04