Stearoyl chloride → HCID 70359046、化合物
反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:16]=[CH:17][CH:18]=1)[CH:6]([OH:15])[C:7](=[O:14])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.C(Cl)(=O)CCCCCCCCCCCCCCCCC.C1(C(C(C2C=CC=CC=2)O)=O)C=CC=CC=1.C(S([O-])(=O)=O)CCCCCCCCCCCCCCC.F[C:76](F)([C:80](F)(F)[C:81](F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)[C:77]([O-:79])=[O:78]>C(N(CC)CC)C.C1(C)C=CC=CC=1>[C:77]([OH:79])(=[O:78])[CH2:76][CH2:80][CH2:81][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:8][CH2:7][CH2:6][CH2:5][CH2:16][CH2:17][CH2:18][CH2:3][CH3:4].[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:16]=[CH:17][CH:18]=1)[CH:6]([OH:15])[C:7](=[O:14])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1参加物
8
実験手順
3'-Methoxybenzoin (5 g, 0.021 mol) was dissolved in 200 ml of toluene containing one equivalent of triethylamine. One equivalent of octadecanoyl chloride in 20 ml of toluene was added slowly to the cooled (ice bath) stirred benzoin solution. Stirring was continued with ice bath cooling for one hour. The reaction mixture was then filtered free of precipitated amine salt and the filtrate was evaporated to give an oil which solidified to give a low melting solid. The hexadecanesulfonate (Compound 14) and perfluorooctanoate (Compound 15) (m.p. 55°-58° C.) esters were similarly prepared from the corresponding acid chlorides.
後処理
- temperaturecooled (ice bath)
- customwas continued with ice bath
- temperaturecooling for one hour
- filtrationThe reaction mixture was then filtered free of precipitated amine salt
- customthe filtrate was evaporated
- customto give an oil which
- customto give a low melting solid
出典と根拠
- ORDレコード
- ord-416b98a08c984043b5c0db4327ba5941
- 出典データセット
- uspto-grants-1986_07
- 特許番号
- US04599273
反応ノート
読み込み中…