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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2417745생성일: 2026년 10월 26일

Hydrochloric Acid → 2-(Naphthalen-2-yl)-1,3-dithiane

https://huagongshe.com/reaction/2417745

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-NaphthalenecarboxaldehydeHCID 6201—
반응물1,3-PropanedithiolHCID 8013—
반응물Acryloyl chlorideHCID 13140—
반응물2-Phenyl-1,3-dithianeHCID 21547—
반응물1,2-DithioleHCID 525331—
반응물2-(3,5-Dimethoxyphenyl)-2-hydroxy-1-phenyl-ethanoneHCID 555593—
반응물MethoxybenzoinHCID 20154532—
반응물3',5'-Dimethoxybenzoin acrylateHCID 70348650—
용매ChloroformHCID 6212—
생성물2-(Naphthalen-2-yl)-1,3-dithianeHCID 13449802—

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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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04469774
출처 데이터셋uspto-grants-1984_09
ORD IDord-acdb80ef058848cbb5829e8545261bfc
출처 메모uspto-grants-1984_09