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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1872307생성일: 2026년 10월 26일

Triethylamine → 2-methoxy-4-[(E)-2-methoxycarbonyl-vinyl]-phenyl 4-[6-(2-methyl-acryloyloxy)-hexyloxy]-benzoate

https://huagongshe.com/reaction/1872307

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methyl 4-hydroxy-3-methoxy-cinnamateHCID 16830—
반응물Thionyl ChlorideHCID 24386—
반응물4-[6-(2-Methyl-acryloyloxy)-hexyloxy]-benzoateHCID 7021645—
촉매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물2-methoxy-4-[(E)-2-methoxycarbonyl-vinyl]-phenyl 4-[6-(2-methyl-acryloyloxy)-hexyloxy]-benzoateHCID 1832918350.8%

반응 조건

온도90 °C

반응 단계

8.5 g (0.028 mol) of 4-[6-(2-methyl-acryloyloxy)-hexyloxy]-benzoate were treated with 6 ml of thionyl chloride and 3 drops of DMF and the mixture was heated to 90° C. for 2 hours. The excess thionyl chloride was completely removed firstly in a water-jet vacuum and subsequently in a high vacuum. The residual acid chloride was taken up in 20 ml of dichloromethane and slowly added dropwise at 0° C. to a solution of 5.25 g (0.025 mol) of methyl 4-hydroxy-3-methoxy-cinnamate and 4.25 ml of triethylamine in 25 ml of THF. The batch was stirred at room temperature overnight, filtered and the filtrate was evaporated to dryness. The residue was purified by column chromatography on silica gel with dichloromethane/diethyl ether (19:1) and subsequently by recrystallization from ethanol/THF. 6.31 g of 2-methoxy-4-[(E)-2-methoxycarbonyl-vinyl]-phenyl 4-[6-(2-methyl-acryloyloxy)-hexyloxy]-benzoate were isolated as a white powder; m.p. 92-94° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06107427
출처 데이터셋uspto-grants-2000_08
ORD IDord-62f38aa2bfe545c8b5dd6142fcea5a7e
출처 메모uspto-grants-2000_08