반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[OH:8].[CH3:9][O:10][CH2:11]OC.C1(C)C=CC(S(O)(=O)=O)=CC=1.C(N(CC)CC)C>C(Cl)Cl>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][CH2:9][O:10][CH3:11]참가 물질
실험 절차
2-Chlorophenol (96.4 g, 0.75 mol), dimethoxymethane (257.9 g, 3.39 mol) and 750 mg of p-toluenesulfonic acid were dissolved in 1.5 L of methylene chloride and the mixture heated at reflux with stirring under nitrogen for 72 hours in a flask equipped with a Soxhlet extraction apparatus containing 400 g of 3A molecular sieves. The mixture was allowed to cool and 3 ml of triethylamine was added. The mixture was then extracted with 2N sodium hydroxide and the organic phase was dried over magnesium sulfate. Evaporation of the volatiles under reduced pressure left 66.9 g of crude 1-chloro-2-methoxymethoxybenzene as a residue. This was distilled and the fraction boiling at 94° C. and 6.5 mm pressure was collected to obtain 51.3 g (40 percent of theory) of purified product. The proton nmr spectrum was consistent with the assigned structure.
후처리
- temperaturethe mixture heated
- temperatureat reflux
- customequipped with a Soxhlet extraction apparatus
- temperatureto cool
- extractionThe mixture was then extracted with 2N sodium hydroxide
- dry with materialthe organic phase was dried over magnesium sulfate
- customEvaporation of the volatiles under reduced pressure
- waitleft 66.9 g of crude 1-chloro-2-methoxymethoxybenzene as a residue
- distillationThis was distilled
- customthe fraction boiling at 94° C. and 6.5 mm pressure was collected
- customto obtain 51.3 g (40 percent of theory) of purified product
출처 및 근거
- ORD 기록
- ord-56372a4afebc4a3ab84dcdad4135b05a
- 출처 데이터셋
- uspto-grants-1990_12
- 특허 번호
- US04979978
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