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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1849953Erstellt: 26. Oktober 2026

gamma-Butyrolactone methacrylate → 3-Hydroxy-1-methacryloyloxyadamantane

https://huagongshe.com/reaction/1849953

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktgamma-Butyrolactone methacrylateHCID 11206014—
Edukt3-Hydroxy-1-methacryloyloxyadamantaneHCID 11856523—
Edukt2-Propenoic acid, 2-methyl-, 1-ethylcyclopentyl ester (9CI, ACI)HCID 18000579—
Edukt1-Isopropyl-adamantanyl methacrylateHCID 66862563—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Hydroxy-1-methacryloyloxyadamantaneHCID 11856523—
ProduktIam ecpmaHCID 131731389—

Reaktionsschritte

A solution of 1-ethylcyclopentyl methacrylate (ECPMA, M1; 20 mmol), 1-isopropyl-adamantanyl methacrylate (IAM, M2; 20 mmol), 2-oxo-tetrahydro-furan-3-yl methacrylate (α-GBLMA, M3; 30 mmol), 3-oxo-4,10-dioxa-tricyclo[5.2.1.02,6]dec-8(or 9)-yl methacrylate (ODOTMA, M4; 20 mmol), and 3-hydroxy-adamantanyl methacrylate (HAMA, M5; 10 mmol) dissolved in 30 g of tetrahydrofuran (THF) was degassed by bubbling with nitrogen and charged to a 500 ml flask equipped with a condenser, nitrogen inlet and mechanical stirrer along with an additional 10 g of degassed THF. The solution is brought to reflux, and 6 g of dimethyl-2,2-azodiisobutyrate is dissolved in 5 g of THF and charged in to the flask. The polymerization mixture is then stirred for about 4 hours at reflux, after which time the reaction is diluted with 5 g of THF and the polymerization mixture cooled to room temperature. The polymer is precipitated by addition to 1.0 L of isopropanol, the solid collected by filtration, re-precipitated by dissolving in 50 g THF and dropwise addition to another 1.0 L isopropanol, and the precipitated polymer collected and dried under vacuum at 45° C. for 48 h. to yield photoresist polymer poly(IAM/ECPMA/α-GBLMA/ODOTMA/HAMA) (20:20:30:20:10 ratio, respectively). Mw=8,000.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08956799B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-c35fff670b2d45658146bc5328039efc
Quellennotizuspto-grants-2015_02