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HRID 866056作成日:2026年10月27日

Ethyl 4-piperidinecarboxylate → ethyl N-[4-(2-propen-1-yloxy)phenylmethyl]piperidin-4-ylcarboxylate

https://huagongshe.com/reaction/866056

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 4-piperidinecarboxylateHCID 70770—
反応物4-(Allyloxy)benzaldehydeHCID 95942—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物ethyl N-[4-(2-propen-1-yloxy)phenylmethyl]piperidin-4-ylcarboxylateHCID 1904093498.9%

反応手順

The reaction conditions taught by A. E. Moormann, Syn. Comm., 23(6), 789-795 (1993) were used in the following preparation. To a stirred solution of 4.8 grams (0.030 mole) of ethyl piperidin-4-ylcarboxylate and 4.9 grams (0.030 mole) of 4-(2-propen-1-yloxy)benzaldehyde in 50 mL of ethanol was added 3.8 mL (0.030 mole) of borane-pyridine complex. Upon completion of addition, the reaction mixture was stirred at ambient temperature for about 18 hours. The reaction mixture was then taken up in water and extracted with methylene chloride. The organic layer was washed with water and dried with magnesium sulfate. The mixture was filtered and the filtrate concentrated under reduced pressure, yielding 9.0 grams of ethyl N-[4-(2-propen-1-yloxy)phenylmethyl]piperidin-4-ylcarboxylate. The NMR spectrum was consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05569664
出典データセットuspto-grants-1996_10
ORD IDord-3e0acf32c1dd480bbf13d4c2f7d72993
出典メモuspto-grants-1996_10