Trifluoroacetic acid → (Piperidin-4-yloxy)acetic acid methyl ester hydrochloride
反応式
F[C:2](F)(F)C([O-])=O.[NH:8]1[CH2:13][CH2:12][CH:11]([O:14][CH2:15][C:16]([OH:18])=[O:17])[CH2:10][CH2:9]1.FC(F)(F)C(O)=O.S(Cl)([Cl:28])=O>ClCCl.CO>[ClH:28].[NH:8]1[CH2:9][CH2:10][CH:11]([O:14][CH2:15][C:16]([O:18][CH3:2])=[O:17])[CH2:12][CH2:13]1参加物
7
実験手順
By esterifying the trifluoroacetate of 4-piperidinyloxy-acetic acid (prepared by treating the product of Example 1c) with trifluoroacetic acid in dichloromethane) in methanol in the presence of thionyl chloride there is obtained methyl 4-piperidinyloxyacetate hydrochloride, MS (EI): 173 (M)+.
後処理
- customprepared
出典と根拠
- ORDレコード
- ord-49b97071c3424f3b9a76909d0eae833d
- 出典データセット
- uspto-grants-1996_08
- 特許番号
- US05545658
反応ノート
読み込み中…