Hydrochloric Acid → 1-[3-(3,5-Bistrifluoromethylphenyl)-2-propynyl]piperidine hydrochloride
反応式
[ClH:1].[F:2][C:3]([F:24])([F:23])[C:4]1[CH:5]=[C:6]([C:14]#[C:15][CH2:16][N:17]2[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)[CH:7]=[C:8]([C:10]([F:13])([F:12])[F:11])[CH:9]=1>C(OCC)C>[ClH:1].[F:13][C:10]([F:11])([F:12])[C:8]1[CH:7]=[C:6]([C:14]#[C:15][CH2:16][N:17]2[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22]2)[CH:5]=[C:4]([C:3]([F:23])([F:24])[F:2])[CH:9]=1参加物
4
実験手順
An excess of dry HCl gas was passed through a solution of 1-(3,5-bistrifluoromethylphenyl)-3-piperidinoprop-1-yne (2.26 g) in dry diethyl ether (200 ml). Filtration, washing (diethyl ether) and drying of the resulting white precipitate gave 2.16 g of a fine white powder of melting point 214.5° C.
後処理
- filtrationFiltration
- washwashing (diethyl ether)
- customdrying of the resulting white precipitate
出典と根拠
- ORDレコード
- ord-ed06c24c01b04411accf6dff0f2cccde
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07084158B2
反応ノート
読み込み中…