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HRID 271630作成日:2026年10月27日

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

https://huagongshe.com/reaction/271630

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物NitrobenzeneHCID 7416—
反応物Bis(dichloromethyl) etherHCID 558102—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物1,2-Bis(2-methyl-1-benzothiophen-3-yl)cyclopenteneHCID 15351452—
生成物1,2-Bis(2-methyl-6-formyl-1-benzothiophen-3-yl)cyclopenteneHCID 58738335—

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07452950B2
出典データセットuspto-grants-2008_11
ORD IDord-12f474d27795466daff41c8b2715e52c
出典メモuspto-grants-2008_11