참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | gamma-Butyrolactone methacrylate | HCID 11206014 | — |
| 반응물 | 3-Hydroxy-1-methacryloyloxyadamantane | HCID 11856523 | — |
| 반응물 | 2-Propenoic acid, 2-methyl-, 1-ethylcyclopentyl ester (9CI, ACI) | HCID 18000579 | — |
| 반응물 | 1-Isopropyl-adamantanyl methacrylate | HCID 66862563 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-Hydroxy-1-methacryloyloxyadamantane | HCID 11856523 | — |
| 생성물 | Iam ecpma | HCID 131731389 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08956799B2 |
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| 출처 데이터셋 | uspto-grants-2015_02 |
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| ORD ID | ord-c35fff670b2d45658146bc5328039efc |
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| 출처 메모 | uspto-grants-2015_02 |
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