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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 352269생성일: 2026년 10월 25일

Triethylamine → 5-[4-(6-Acryloyloxyhexyloxy)benzoyloxy]-2-hydroxybenzoic acid 6-acryloyloxyhexyl ester

https://huagongshe.com/reaction/352269

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물4-((6-(Acryloyloxy)hexyl)oxy)benzoic acidHCID 3713565—
반응물2,5-Dihydroxybenzoic-6-acryloyloxyhexyl esterHCID 22709075—
용매TetrahydrofuranHCID 8028—
생성물5-[4-(6-Acryloyloxyhexyloxy)benzoyloxy]-2-hydroxybenzoic acid 6-acryloyloxyhexyl esterHCID 20730921—

반응 조건

온도-25 °C

반응 단계

A solution of mesyl chloride (3.44 g) in 50 ml of dry THF was added dropwise under argon to a cooled (−25° C.) solution of 4-(6-acryloyloxyhexyloxy)benzoic acid (8.35 g) and triethylamine (6.07 g) in 100 ml of dry THF. After complete addition (15 min), the reaction mixture was stirred for a further 30 min at −25° C., treated with a solution of 2,5-dihydroxybenzoic-6-acryloyloxyhexyl ester in 50 ml of dry THF and further stirred at −25° C. for 4 h. The reaction mixture was then filtered through celite and the solvent was removed by evaporation. The filtrate was purified by flash chromatography using a short silica-gel column and dichloromethane/diethylether (39/1) as eluent to give 10.8 g of 5-[4-(6-acryloyloxyhexyloxy)benzoyloxy]-2-hydroxybenzoic acid 6-acryloyloxyhexyl ester as a slightly beige oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06746729B1
출처 데이터셋uspto-grants-2004_06
ORD IDord-551d57505b434dd1ad09a0e8ce9c6206
출처 메모uspto-grants-2004_06