반응식
[F:1][C:2]([F:15])([F:14])[C:3]1[CH:4]=[C:5]([C:9]2[O:10][CH:11]=[CH:12][CH:13]=2)[CH:6]=[CH:7][CH:8]=1.C([Li])CCC.[CH2:21]=[O:22].Cl>O1CCCC1>[OH:22][CH2:21][C:11]1[O:10][C:9]([C:5]2[CH:6]=[CH:7][CH:8]=[C:3]([C:2]([F:1])([F:14])[F:15])[CH:4]=2)=[CH:13][CH:12]=1참가 물질
반응 조건
- 온도
- -40 °C
실험 절차
2-(3-Trifluoromethylphenyl)-furan (J. Chem. Soc. (C) 1968, 2737 and Acta Chem Scand. 24, 2379 (1970))(21.2 g; 0.1 mole) was stirred in tetrahydrofuran (100 ml), cooled to -40° C. and n-butyl lithium (0.1 mole, solution in hexane) was added dropwise. After stirring for 1 hour at -40° C., paraformaldehyde (3.3 g; 0.11 mole) was added gradually. The mixture was stirred at -40° C. for 30 minutes, then the temperature was allowed to rise. At 10° C. an exothermic reaction set in and the temperature gradually rose to 40° C. (over 10 minutes), then gradually fell back to 20° C. After stirring for further 1 hour the clear brown solution was poured onto ice/water, adjusted to pH ca 4 with dilute hydrochloric acid and extracted via ethyl acetate. The dried acetate extract (MgSO4) was evaporated to give a brownish yellow viscous oil which was distilled in vacuo to give 2-hydroxymethyl-5-(3-trifluoromethylphenyl)-furan as a colourless liquid b.p. 125° C./0.5 mm., (16.2 g), which on standing gave crystals, m.p. 45° C.
후처리
- stirringThe mixture was stirred at -40° C. for 30 minutes
- customAt 10° C. an exothermic reaction
- customgradually rose to 40° C.
- custom(over 10 minutes)
- customgradually fell back to 20° C
- stirringAfter stirring for further 1 hour the clear brown solution
- additionwas poured onto ice/water
- extractionextracted via ethyl acetate
- extractionThe dried acetate extract (MgSO4)
- customwas evaporated
- customto give a brownish yellow viscous oil which
- distillationwas distilled in vacuo
출처 및 근거
- ORD 기록
- ord-dc94b9fab5b449838cdeabbfa96f6b64
- 출처 데이터셋
- uspto-grants-1978_10
- 특허 번호
- US04123529
연결된 노트
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