反応式
[C:1]([C:5]1[C:6]([N+:17]([O-])=O)=[CH:7][C:8]2[O:12][C:11](=[O:13])[C:10]([CH3:15])([CH3:14])[C:9]=2[CH:16]=1)([CH3:4])([CH3:3])[CH3:2]>[Pd].CO>[NH2:17][C:6]1[C:5]([C:1]([CH3:4])([CH3:3])[CH3:2])=[CH:16][C:9]2[C:10]([CH3:15])([CH3:14])[C:11](=[O:13])[O:12][C:8]=2[CH:7]=1参加物
実験手順
Palladium on carbon (wet; 5 wt %) was placed into a round bottomed flask under nitrogen flow. 5-tert-butyl-3,3-dimethyl-6-nitro-benzofuran-2-one (4.7 g, 17.85 mmol) was then added to the vessel. Methanol (120 mL) was then carefully charged to the vessel under nitrogen atmosphere. The vessel was then purged with N2, evacuated, then charged with hydrogen gas. The vessel was evacuated and re-charged with hydrogen gas, and then a continuous hydrogen gas stream was introduced. After completion, the reaction was filtered through Celite® and the cake was washed with MeOH (300 ml). The solvent was removed in vacuo and the product dried under high vacuum to give a white crystalline solid. 1H-NMR (400 MHZ, DMSO-d6) δ 7.05 (s, 1H); 6.48 (s, 1H); 5.02 (s, 2H, NH2); 1.34 (s, 6H); 1.30 (s, 9H)
後処理
- customThe vessel was then purged with N2
- customevacuated
- additioncharged with hydrogen gas
- customThe vessel was evacuated
- additionre-charged with hydrogen gas
- additiona continuous hydrogen gas stream was introduced
- filtrationAfter completion, the reaction was filtered through Celite®
- washthe cake was washed with MeOH (300 ml)
- customThe solvent was removed in vacuo
- customthe product dried under high vacuum
- customto give a white crystalline solid
出典と根拠
- ORDレコード
- ord-d68a15a449494f4b91e6b0f4448e7b90
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08835639B2
関連ノート
読み込み中…