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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471323Generated: October 26, 2026

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

https://huagongshe.com/reaction/1471323

Reaction equation

Participants

RoleNameHCIDCharge
Reactantgamma-Butyrolactone methacrylateHCID 11206014—
Reactant3-Hydroxy-1-methacryloyloxyadamantaneHCID 11856523—
Reactant2-Propenoic acid, 2-methyl-, 1-ethylcyclopentyl ester (9CI, ACI)HCID 18000579—
Reactant1-Isopropyl-adamantanyl methacrylateHCID 66862563—
SolventTetrahydrofuranHCID 8028—
Product3-Hydroxy-1-methacryloyloxyadamantaneHCID 11856523—
ProductIam ecpmaHCID 131731389—

Reaction Steps

A photoresist polymer for use in the lithographic evaluations (below) is prepared according to the following procedure. A solution of 1-isopropyl-adamantanyl methacrylate (IAM) (20 mmol), 1-ethylcyclopentyl methacrylate (ECPMA)(20 mmol), 2-oxo-tetrahydro-furan-3-yl methacrylate (α-GBLMA) (30 mmol), 3-oxo-4,10-dioxa-tricyclo[5.2.1.02,6]dec-8(or 9)-yl methacrylate (ODOTMA) (20 mmol), and 3-hydroxy-adamantanyl methacrylate (HAMA) (10 mmol) dissolved in 30 g of tetrahydrofuran (THF) is 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 5 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, collected by filtration, re-precipitated by dissolving in 50 g THF and addition to another 1.0 L isopropanol, and collected and dried under vacuum at 45° C. for 48 h. to yield photoresist polymer poly(IAM/ECPMA/α-GBLMA/ODOTMA/HAMA). Mw=9,000.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012128B2
Source datasetuspto-grants-2015_04
ORD IDord-7903ced116f34756870b0c91cf84a2c8
Source noteuspto-grants-2015_04