돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 988936생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/988936

반응식

참여 물질

역할이름HCID투입량
반응물3-BromophenolHCID 11563—
반응물Potassium HydroxideHCID 14797—
반응물2-NaphthylalanineHCID 185915—
반응물1-Chloro-3,7-dimethyloctaneHCID 227360—
용매EthanolHCID 702—
생성물3-(3,7-Dimethyloctyloxy)bromobenzeneHCID 18004181—

반응 조건

온도32.5 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06638646B2
출처 데이터셋uspto-grants-2003_10
ORD IDord-7b4334bc727e4fd09c7d8cae82bd40f8
출처 메모uspto-grants-2003_10