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HRID 509177作成日:2026年10月27日

4-Bromobenzaldehyde → p-Bromobenzhydryl alcohol

https://huagongshe.com/reaction/509177

反応式

関与物質

役割名称HCID仕込み量
反応物4-BromobenzaldehydeHCID 70741—
反応物HCID 178418255HCID 178418255—
溶媒TetrahydrofuranHCID 8028—
生成物p-Bromobenzhydryl alcoholHCID 9822165.1%

反応手順

To a solution of p-bromobenzaldehyde 10 (4 g, 21.6 mmol) in THF (20 mL) was added phenyl magnesium bromide (22.7 mL, 22.7 mmol) and the reaction mixture was stirred at room temperature for 30 minutes, quenched with water and partially concentrated under vacuum. The crude material was dissolved in ethyl acetate and washed with water. The organic layer was separated, dried over Na2SO4, filtered and concentrated. The residue was purified via prep-HPLC (ISCO) in silica gel column with a gradient of ethyl acetate (5-45%) in hexanes to afford title compound 11 as a colorless oil (3.7 g, 65%). 1H NMR (DMSO-d6) δ (ppm): 7.49-7.45 (m, 2H), 7.36-7.17 (m, 7H), 5.98 (d, J=4.1 Hz, 1H), 5.68 (d, J=3.9 Hz, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09096565B2
出典データセットuspto-grants-2015_08
ORD IDord-7bfae734ebab4c12836f611a56949d96
出典メモuspto-grants-2015_08