참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 2-Naphthalenecarboxaldehyde | HCID 6201 | — |
| 반응물 | 1,3-Propanedithiol | HCID 8013 | — |
| 반응물 | Acryloyl chloride | HCID 13140 | — |
| 반응물 | 2-Phenyl-1,3-dithiane | HCID 21547 | — |
| 반응물 | 1,2-Dithiole | HCID 525331 | — |
| 반응물 | 2-(3,5-Dimethoxyphenyl)-2-hydroxy-1-phenyl-ethanone | HCID 555593 | — |
| 반응물 | Methoxybenzoin | HCID 20154532 | — |
| 반응물 | 3',5'-Dimethoxybenzoin acrylate | HCID 70348650 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 2-(Naphthalen-2-yl)-1,3-dithiane | HCID 13449802 | — |
반응 단계
The special characteristic of the polymeric compound of the invention is the methoxybenzoin (3'-; 3',4'-; or 3',5'-) group of the polymer. The compound is photosensitive per se without the presence of other photosensitive groups. The precursors of a polymeric compound, e.g., poly(3',5'-dimethoxybenzoinacrylate), are set forth in Example 1 below. For example, 2-phenyl-1,3-dithiane is prepared as described by Seebach et al., J. Org. Chem. 31, 4303 (1966). This compound is then used to prepare 2-[1-hydroxy-1-(3,5-dimethoxyphenyl)]methyl-2-phenyl-1,3-dithiane by the general procedure described by Seebach et al., J. Org. Chem. 40, 231 (1975). 3',5'-dimethoxybenzoin is subsequently prepared by thioketal hydrolysis according to the general procedure described by Naraska et al., Bull. Chem. Soc. Japan (Tokyo), 45, 3724 (1972). This compound is esterified to 3',5'-dimethoxybenzoin acrylate by known esterification procedures using acryloyl chloride and then is polymerized in a known way to form a polymer of the invention. An alternative procedure for preparing a substituted benzoin acrylate monomer illustrated in Example 3 is as follows: an aldehyde, e.g., β-naphthaldehyde and a dithiol, e.g., 1,3-propanedithiol, are reacted in a solvent, e.g., chloroform saturated with HCl, to form 2-β-naphthyl-1,3-dithiane. To the isolated product in anhydrous tetrahydrofuran is added n-butyllithium/hexane at dry ice/acetone temperature. Subsequently 3,5-dimethoxybenzaldehyde in the same solvent is added and stirred followed 30 minutes later by acryloyl chloride in solvent to form 3,4-benzo-3',5'-dimethoxybenzoin acrylate thioketal. Hydrolysis of the thioketal as described above produces 3,4-benzo-3',5'-dimethoxybenzoin acrylate. It is recognized that analogues of the above compounds can be prepared by the foregoing procedures. The proportions of the various repeating units in the final copolymer can be controlled by controlling the quantities of reactants present during copolymerization.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04469774 |
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| 출처 데이터셋 | uspto-grants-1984_09 |
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| ORD ID | ord-acdb80ef058848cbb5829e8545261bfc |
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| 출처 메모 | uspto-grants-1984_09 |
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