반응식
[O:1]([CH2:8][CH2:9]O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1(C)C=CC=CC=1.S(Cl)([Cl:20])=O>N1C=CC=CC=1>[Cl:20][CH2:9][CH2:8][O:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1참가 물질
5
실험 절차
To a flask was added 41.5 grams (g.) (0.3 mole) of 2-phenoxyethanol, 50 ml of toluene and 3.93 g. of pyridine, then 39.3 g. (0.33 mole) of thionyl chloride dropwise while stirring at room temperature. The exothermic reaction was heated at 50°-60° C. for two hours. After cooling to room temperature, the resulting salt was filtered and washed with methylene chloride. The filtrate was washed several times with aqueous sodium bicarbonate, dried using sodium sulfate, and then concentrated to obtain 39 g. of the 1-chloro-2-phenoxyethane as a yellow oil (83% yield).
후처리
- customThe exothermic reaction
- temperaturewas heated at 50°-60° C. for two hours
- filtrationthe resulting salt was filtered
- washwashed with methylene chloride
- washThe filtrate was washed several times with aqueous sodium bicarbonate
- customdried
- concentrationconcentrated
- customto obtain 39 g
출처 및 근거
- ORD 기록
- ord-a5f09de4d0fd4c8084623f9223aa0406
- 출처 데이터셋
- uspto-grants-1996_06
- 특허 번호
- US05527816
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