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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 990168생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/990168

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 단계

450 ml of ethanol were placed in the reaction vessel and admixed with Nal (10.5 g; 70 mmol) and KOH (67.3 g; 1.2 mol). A temperature rise from 25 to 40° C. was observed after addition of the KOH. After cooling to room temperature, 3-bromophenol (175.5 g; 1 mol) was added. The white suspension became beige during this addition. 3,7-dimethyloctyl chloride (186.32 g; 212.94 ml; 1.05 mol) was added over a period of 3 minutes by means of a dropping funnel. The mixture was stirred further for 2 hours at RT and subsequently for 96 hours at an internal temperature of 80° C. 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, washed once with H2O, three times with H2O which had been acidified with CO2 and again with H2O. After drying over MgSO4, the solvent was again taken off on a rotary evaporator and the crude product was purified by fractional vacuum distillation.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06458909B1
출처 데이터셋uspto-grants-2002_10
ORD IDord-cbc7c7afb4c94357abc088835cb8dc80
출처 메모uspto-grants-2002_10