[1-(2,5-Dichlorophenyl)-cyclopentyl]-acetonitrile → (1-Naphthalen-2-yl-cyclopentyl)-acetonitrile
反応式
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11]1([CH2:16]OS(C)(=O)=O)[CH2:15][CH2:14][CH2:13][CH2:12]1.ClC1C=CC(Cl)=CC=1C1(C[C:36]#[N:37])CCCC1>>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11]1([CH2:16][C:36]#[N:37])[CH2:15][CH2:14][CH2:13][CH2:12]1参加物
3
実験手順
(1-Naphthalen-2-yl-cyclopentyl)-acetonitrile (215) (9.0 g, 72.67%) was synthesized as a brown solid from methanesulfonic acid 1-naphthalen-2-yl-cyclopentylmethyl ester 214) (16.0 g, 52.63 mmol) following the procedure described for [1-(2,5-dichlorophenyl)-cyclopentyl]-acetonitrile (202).
出典と根拠
- ORDレコード
- ord-eb1b27f9b85a40eeb64b9d1671e0c03d
- 出典データセット
- uspto-grants-2015_06
- 特許番号
- US09045486B2
反応ノート
読み込み中…