Boron trifluoride etherate → 1-Benzyl 4-ethyl 5-oxoazepane-1,4-dicarboxylate

HRID 1813901ノート

反応式

HRID 1813901 の反応式
[O:1]=[C:2]1[CH2:7][CH2:6][N:5]([C:8]([O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[O:9])[CH2:4][CH2:3]1.[CH2:18]([O:20][C:21](=[O:25])[CH:22]=[N+]=[N-])[CH3:19].B(F)(F)F.CCOCC>CCOCC>[O:1]=[C:2]1[CH2:7][CH2:6][N:5]([C:8]([O:10][CH2:11][C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)=[O:9])[CH2:4][CH2:3][CH:22]1[C:21]([O:20][CH2:18][CH3:19])=[O:25]

参加物

5

反応物 3

HCID 8000Boron trifluoride etherateHCID 12192Ethyl diazoacetateHCID 643496Benzyl 4-oxopiperidine-1-carboxylate

生成物 1

HCID 146001211-Benzyl 4-ethyl 5-oxoazepane-1,4-dicarboxylate収率 88%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

反応条件

温度
-45 °C

実験手順

A dry 500 ml 3-neck flask was charged with benzyl 4-oxo-1-piperidinecarboxylate (35.08 g, 150 mmol). It was dissolved in 130 ml Et2O and cooled to −45° C. Ethyldiazoacetate (20.5 ml, 195 mmol) and boron trifluoride ethyl ether (19.4 ml, 158 mol) were added simultaneously by syringe pump over 45 minutes. The temperature was kept below −25° C. The reaction was stirred for 30 minutes longer, and then quenched with sat. NaHCO3. The ice bath was removed. The reaction was diluted with EtOAc (250 ml) and H2O (150 ml). The layers were separated, and the organic phase was dried over MgSO4. It was concentrated under reduced pressure to an orange oil. The product was purified by flash chromatography (silica gel, 40% EtOAc/hexane), yielding product as pale yellow oil (42.1 g, 88%). 1H NMR (CDCl3)δ 67.39-7.31, 5.15-5.12, 4.42-4.17, 3.96-3.83, 3.75-3.70, 3.65, 3.54-3.37, 2.08-2.03, 1.29-1.24; IR (liq.) 1743, 1702, 1476, 1455, 1443, 1425, 1371, 1318, 1295, 1238, 1213, 1178, 1098, 1068, 1028 cm−1.

後処理

  1. customwas kept below −25° C
  2. customquenched with sat. NaHCO3
  3. customThe ice bath was removed
  4. additionThe reaction was diluted with EtOAc (250 ml) and H2O (150 ml)
  5. customThe layers were separated
  6. dry with materialthe organic phase was dried over MgSO4
  7. concentrationIt was concentrated under reduced pressure to an orange oil
  8. customThe product was purified by flash chromatography (silica gel, 40% EtOAc/hexane)

出典と根拠

ORDレコード
ord-ac4544eaa4b6400e9b07205adfffec85
出典データセット
uspto-grants-2005_04
特許番号
US06875762B2

反応ノート

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