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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 271630생성일: 2026년 10월 26일

Water → 1,2-Bis(2-methyl-6-formyl-1-benzothiophen-3-yl)cyclopentene

https://huagongshe.com/reaction/271630

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물NitrobenzeneHCID 7416—
반응물Bis(dichloromethyl) etherHCID 558102—
반응물Aluminum(III) ChlorideHCID 6451240—
반응물1,2-Bis(2-methyl-1-benzothiophen-3-yl)cyclopenteneHCID 15351452—
생성물1,2-Bis(2-methyl-6-formyl-1-benzothiophen-3-yl)cyclopenteneHCID 58738335—

반응 조건

온도0 °C

반응 단계

Dichloromethyl ether (4.52 ml, 50 mmol) and anhydrous aluminum chloride (1.78 g, 13.35 mmol) were added to a stirred solution of 1,2-bis(2-methyl-1-benzothiophen-3-yl)cyclopentene 4 (1.2 g, 3.33 mmol) in nitrobenzene (25 ml) at 0° C., and the mixture was stirred for 30 min at 0° C. and for 20 hours at room temperature. The reaction mixture was poured into icy water, and the product was extracted by ethyl acetate, was washed with water and was dried by magnesium sulfate. After distillation of nitrobenzene under vacuum, the product was purified by the column chromatography (Silica Gel, 0.063-0.1) with a petroleum ether (40/70):ethyl acetate mixture (6:1 by volume) being used as an eluent. The yield was 0.56 g of dialdehyde 5 (40%), Tmelt=196-197° C. (hexane:chloroform, 6:1 by volume). Mass spectrum, m/z: 416, [M]+. A 1H NMR spectrum (DMSO-d6, δ, ppm, J/Hz): 2.25 (m, 6H, 2×CH3), 2.97 (br m, 6H, 3×CH2), 7.6-8.5 (br m, 6H, CHarom.), 9.98 (br m, 2H, 2×CHO). The results found (%): C, 72.16; H, 4.86; S, 15.34. C25H20O2S2. The results calculated (%): C, 72.08; H, 4.84; S, 15.40.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07452950B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-12f474d27795466daff41c8b2715e52c
출처 메모uspto-grants-2008_11