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HRID 1353121作成日:2026年10月27日

Phenyl cyanate → 4-Cyclopentyl-but-2-ynenitrile

https://huagongshe.com/reaction/1353121

反応式

関与物質

役割名称HCID仕込み量
反応物Phenyl cyanateHCID 70740—
反応物(Prop-2-yn-1-yl)cyclopentaneHCID 521007—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
生成物4-Cyclopentyl-but-2-ynenitrileHCID 2110231747%

反応条件

温度-78 °C

反応手順

Prop-2-ynyl-cyclopentane (46.2 mmol) was dissolved in 100 mL of anhydrous Et2O under N2 and the reaction was cooled to −78° C. A 2.5 M solution of BuLi in hexanes (55.5 mmol) was added dropwise to the reaction over 30 minutes. The reaction was stirred for an additional 20 minutes and phenyl cyanate (55.5 mmol) was then added in solution with 20 mL of Et2O dropwise over 20 minutes. The resultant solution was allowed to slowly warm to rt and stir for 3 hours. The reaction material was then diluted in 200 mL of fresh Et2O and washed with three 100 mL portions of 1 N aqueous NaOH solution. The organics were then washed with 200 mL of brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified through flash chromatography on silica gel to give 4-cyclopentyl-but-2-ynenitrile (21.7 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07220865B2
出典データセットuspto-grants-2007_05
ORD IDord-58662001d63c48e79d3be55517eee19b
出典メモuspto-grants-2007_05