cis Ethyl 3-bromo-2-oxo-1-azacyclodecane-10-carboxylate → cis Ethyl 3-acetoxy-2-oxo-1-azacyclodecane-10-carboxylate

HRID 5392

反応式

Br[C@H:2]1[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][C@@H:5]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[NH:4][C:3]1=[O:17]>CN(C)C=O.C(OCC)(=O)C.C([O-])(=O)C.[Ag+]>[C:12]([O:14][C@H:2]1[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][C@@H:5]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[NH:4][C:3]1=[O:17])(=[O:13])[CH3:5]

参加物

反応条件

温度: 100 °C

実験手順

Cis ethyl 3-bromo-2-oxo-1-azacyclodecane-10-carboxylate (2.96 g, 9.67 mmol) is dissolved in dimethylformamide (30 mL). Silver acetate (6.35 g, 38 mmol) is added, and the reaction is heated to 100° C. for 3 hours. After cooling back to room temperature, the reaction is diluted with ethyl acetate (100 mL), filtered through a pad of silica gel, and the solvent is evaporated to give crude cis ethyl 3-acetoxy-2-oxo-1-azacyclodecane-10-carboxylate.

後処理

temperatureAfter cooling back to room temperature
filtrationfiltered through a pad of silica gel
customthe solvent is evaporated

出典と根拠

ORDレコード: ord-dcb68cc3bff744d997cc097884f62d34
出典データセット: uspto-grants-1993_09
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US05244889

反応式

参加物

反応物 1

生成物 1

試薬・触媒・溶媒 3

反応条件

実験手順

後処理

出典と根拠

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