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HRID 988936作成日:2026年10月27日

3-Bromophenol → 3-(3,7-Dimethyloctyloxy)bromobenzene

https://huagongshe.com/reaction/988936

反応式

関与物質

役割名称HCID仕込み量
反応物3-BromophenolHCID 11563—
反応物Potassium HydroxideHCID 14797—
反応物2-NaphthylalanineHCID 185915—
反応物1-Chloro-3,7-dimethyloctaneHCID 227360—
溶媒EthanolHCID 702—
生成物3-(3,7-Dimethyloctyloxy)bromobenzeneHCID 18004181—

反応条件

温度32.5 °C

反応手順

450 ml of ethanol were initially introduced, and Nal (10.5 g; 70 mmol) and KOH (67.3 g; 1.2 mol) were added. A temperature increase from 25 to 40° C. after addition of the KOH was observed. After the mixture had been cooled to room temperate, 3-bromophenol (176.5 g; 1 mol) was added, during which the white suspension became beige. 3,7-Dimethyloctyl chloride (186.32 g; 212.94 ml; 1.05 mol) was added over the course of 3 minutes via a dropping funnel. The mixture was stirred at RT for a further 2 hours and subsequently stirred at an internal temperature of 80° C. for 96 hours. Ethanol was distilled off. The residue was taken up in ethyl acetate, and the precipitate was separated off by filtration. The organic phase was extracted three times with 10% strength by weight aqueous NaOH solution and washed once with H2O, three times with H2O which had been acidified using CO2 and again with H2O. After the mixture had been dried using MgSO4, the solvent was stripped off again in a rotary evaporator, and the crude product was purified by fractional distillation under reduced pressure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06638646B2
出典データセットuspto-grants-2003_10
ORD IDord-7b4334bc727e4fd09c7d8cae82bd40f8
出典メモuspto-grants-2003_10