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HRID 29269作成日:2026年10月26日

Isopropyl iodide → 1-Bromo-3-(isopropylsulfanyl)benzene

https://huagongshe.com/reaction/29269

反応式

関与物質

役割名称HCID仕込み量
反応物Isopropyl iodideHCID 6362—
反応物Potassium CarbonateHCID 11430—
反応物m-BromobenzenethiolHCID 80597—
溶媒AcetoneHCID 180—
生成物1-Bromo-3-(isopropylsulfanyl)benzeneHCID 1797877293.17%

反応手順

3-Bromobenzenethiol (1 g, 5.3 mmol) was added to acetone (25 mL). Next was added potassium carbonate (1.46 g, 10.58 mmol) and 2-iodopropane (1.17 g, 6.88 mmol). This was refluxed for 5 h. Reaction was then cooled to rt and filtered through a pad of Celite. The organic was then concentrated in vacuo and taken up in ether at which time a white precipitate crashed out. The organic was then re-filtered through the same celite plug and concentrated in vacuo to provide 1.14 g (93.17%) of 1-bromo-3-isopropylsulfanyl-benzene as an oil. 1H-NMR (methylene chloride -d2) δ 7.54 (s, 1H), 7.37-7.31 (m, 2H), 7.18 (t, J=7.9 Hz, 1H), 3.50-3.36 (m, 1H), 1.31 (d, J=6.1 Hz, 6H); LC-MS RT: 4.15, [M+H]+: 233.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420066B2
出典データセットuspto-grants-2008_09
ORD IDord-93ef0c03cac1401c888e831169151d18
出典メモuspto-grants-2008_09