Benzyl N-[(oxolan-3-yl)methyl]carbamate → (R)-benzyl (tetrahydrofuran-3-yl)methylcarbamate
反応式
[O:1]1[CH2:5][CH2:4][CH:3]([CH2:6][NH:7][C:8](=[O:17])[O:9][CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH2:2]1>O1CCCC1>[O:1]1[CH2:5][CH2:4][C@H:3]([CH2:6][NH:7][C:8](=[O:17])[O:9][CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH2:2]1.[O:1]1[CH2:5][CH2:4][C@@H:3]([CH2:6][NH:7][C:8](=[O:17])[O:9][CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH2:2]1参加物
4
実験手順
A racemic mixture of benzyl (tetrahydrofuran-3-yl)methylcarbamate was dissolved in tetrahydrofuran and separated by liquid chromatography with a Chiralpak IC 2.5 cm ID×25 cm, 20 micron column, eleuting with hexane/tetrahydrofuran/isopropanol (85/10/5), to provide (R)-benzyl (tetrahydrofuran-3-yl)methylcarbamate and (S)-benzyl (tetrahydrofuran-3-yl)methylcarbamate.
後処理
- customseparated by liquid chromatography with a Chiralpak IC 2.5 cm ID×25 cm, 20 micron column
出典と根拠
- ORDレコード
- ord-4f13e52836854f93b89bbe6fbb083615
- 出典データセット
- uspto-grants-2016_04
- 特許番号
- US09302989B2
反応ノート
読み込み中…