Cyclohexylammonium Ion → 2,2-Dimethyl-5-indanacetic acid

反応式

C[O:2][C:3](=[O:17])[C:4](=O)[C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[CH2:10][C:9]([CH3:15])([CH3:14])[CH2:8]2.C1([NH3+])CCCCC1>>[CH3:14][C:9]1([CH3:15])[CH2:8][C:7]2[C:11](=[CH:12][CH:13]=[C:5]([CH2:4][C:3]([OH:17])=[O:2])[CH:6]=2)[CH2:10]1

参加物

反応物 2

HCID 1549093Cyclohexylammonium Ion

HCID 545199402,2-Dimethyl-alpha-oxo-5-indanacetic acid methyl ester

生成物 1

HCID 132398922,2-Dimethyl-5-indanacetic acid

実験手順

2,2-dimethyl-α-oxo-5-indanacetic acid methyl ester is reduced in a manner analogous to that described in Example 4. The cyclohexyl-ammonium salt of the title compound has an M.P. of 155°-156°.

出典と根拠

ORDレコード: ord-3d2e775d92d84bda91804d294a3222d8
出典データセット: uspto-grants-1979_08
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US04166131

反応ノート

読み込み中…