反応式
[CH3:1][C@@H:2]1O[C@H:3]1[CH2:5]O.CC1C=CC(S([O-])(=O)=O)=CC=1.[Li]CCCC.[O:23]([C:30]([NH:32][O:33][C:34]([O:36][C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1)=[O:35])=[O:31])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CCOC(/N=N/C(OCC)=O)=O>C1COCC1.C(O)(=O)C>[O:23]([C:30]([N:32]([C@@H:3]([C:2]#[CH:1])[CH3:5])[O:33][C:34]([O:36][C:37]1[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=1)=[O:35])=[O:31])[C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
A solution of (2S-trans)-3-methyloxiranemethanol 4-methylbenzenesulfonate (484 mg; 2 mmol), prepared as in step 1, in dry THF (20 ml) was treated at -70° C. to -60° C. with n-BuLi (1.6M in hexane, 7.5 ml, 12 mmol) under an atmosphere of nitrogen. Glacial acetic acid (1 ml) was added after consumption of all the rosylate (monitored by TLC). After 15 min, sodium bicarbonate (600 mg) was added and the reaction mixture was allowed to warm to room temperature. After filtration through Celite, N,O-diphenoxycarbonylhydroxylamine (550 mg, 2.00 mmol) and triphenylphosphine (786 mg, 3.00 mmol) were added to the filtrate. The resulting mixture was treated with DEAD (0.5 ml, 3.0 mmol), taking care that the reaction temperature did not rise above ambient temperature. The reaction mixture was stirred at room temperature for 16 hours and then concentrated in vacuo. The residue was purifed by chromatography on silica-gel (10% ethyl acetate/hexane) to give (R)-N,O-bis(phenoxycarbonyl)-N-(3-butyn-2-yl)hydroxylamine(contaminated with phenol).
後処理
- customafter consumption of all the rosylate (monitored by TLC)
- additionsodium bicarbonate (600 mg) was added
- additionwere added to the filtrate
- customdid not rise above ambient temperature
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-8acfe5972ea34b25acf7ac20ff24aeb6
- 出典データセット
- uspto-grants-1997_04
- 特許番号
- US05616596
関連ノート
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