Thionyl Chloride → HCID 20344102、化合物
反応式
[F:1][C:2]1[CH:3]=[C:4]([CH:14]=[CH:15][CH:16]=1)[O:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[CH2:12]O.S(Cl)([Cl:19])=O>N1C=CC=CC=1>[Cl:19][CH2:12][C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=1[O:5][C:4]1[CH:14]=[CH:15][CH:16]=[C:2]([F:1])[CH:3]=1参加物
4
実験手順
2-(3-Fluorophenoxy)benzenemethanol (30 g.) was mixed with 13.2 ml. of pyridine. Thionyl chloride (12.4 ml.) was added dropwise at 25°-30°, the mixture stirred 5 hours at room temperature, then partitioned between water and ether. The organic layer was washed with a 10% sodium carbonate solution, then with water, dried over sodium carbonate and evaporated to give the title compound. ##STR12##
後処理
- custompartitioned between water and ether
- washThe organic layer was washed with a 10% sodium carbonate solution
- dry with materialwith water, dried over sodium carbonate
- customevaporated
出典と根拠
- ORDレコード
- ord-76b9dd455a514ed2b6d700ed7ef59965
- 出典データセット
- uspto-grants-1980_04
- 特許番号
- US04198421
反応ノート
読み込み中…