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HRID 19764作成日:2026年10月24日

1,4-Dibromobenzene → 1-(4-Bromophenyl)cyclobutanol

https://huagongshe.com/ja/reaction/19764

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DibromobenzeneHCID 7804—
反応物CyclobutanoneHCID 14496—
反応物Ammonium ChlorideHCID 25517—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物1-(4-Bromophenyl)cyclobutanolHCID 1209541934.3%

反応条件

温度-78 °C

反応手順

To a solution of 1,4-dibromobenzene (1.00 g, 4.24 mmol) at −78° C. in ether (20 ml) was added n-BuLi (2.65 ml, 1.6 M solution in hexane, 4.24 mmol) and the reaction mixture was stirred at −78° C. for 30 min. Cyclobutanone (348 μl, 4.66 mmol) was then added and the reaction mixture was stirred at −78° C. for 15 min. The reaction mixture was then slowly (over 2 h) warmed to 0° C. and stirred for a further 1 h. Water was added followed by sat. NH4Cl and the reaction mixture was extracted with ether. The organic layer was washed with brine, dried (MgSO4), filtered and concentrated in vacuo to give a residue which was purified by flash column chromatography (1:4 ether/pentane) to give 1-(4-bromophenyl)-cyclobutanol (330 mg, 34%) as a colorless oil. 1H NMR (CDCl3, 300 MHz): δ 7.50 (d, J=8.5 Hz, 2H), 7.38 (d, J=8.5 Hz, 2H), 2.57-2.48 (m, 2H), 2.41-2.31 (m, 2H), 2.02 (m, 1H), 1.69 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745477B2
出典データセットuspto-grants-2010_06
ORD IDord-d76891fc0c314df8919a1a6861f1cf2a
出典メモuspto-grants-2010_06