反応式
C([O:5][C:6](=[O:17])[CH2:7][CH2:8][C@H:9]([CH3:16])[CH2:10][CH2:11][CH2:12][CH:13]([CH3:15])[CH3:14])(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[CH3:16][C@H:9]([CH2:10][CH2:11][CH2:12][CH:13]([CH3:15])[CH3:14])[CH2:8][CH2:7][C:6]([OH:17])=[O:5]参加物
4
実験手順
(4R)-4,8-dimethyl nonanoic acid t-butyl ester in 25 mL CH2Cl2 at 0° C. was treated with TFA (6 mL). The mixture was allowed to reach ambient temperature and stir overnight. The solvent was removed by rotary evaporation, and the mixture was purified by silica gel chromatography (95/5 hexane/EtOAc) to give 0.962 g (4R)-4,8-dimethyl nonanoic acid. m/z 185 (M−).
後処理
- customto reach ambient temperature
- customThe solvent was removed by rotary evaporation
- customthe mixture was purified by silica gel chromatography (95/5 hexane/EtOAc)
出典と根拠
- ORDレコード
- ord-6857fd771a8b44e0b17585c5501f4bf0
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07419981B2
関連ノート
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