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HRID 222579作成日:2026年10月25日

Chloroacetonitrile → 1-Oxaspiro(2.4)heptane-2-carbonitrile

https://huagongshe.com/reaction/222579

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroacetonitrileHCID 7856—
反応物CyclopentanoneHCID 8452—
反応物Potassium tert-butoxideHCID 23665647—
溶媒tert-ButanolHCID 6386—
生成物1-Oxaspiro(2.4)heptane-2-carbonitrileHCID 54897468.3%

反応手順

A 1 M solution of potassium tert-butoxide in tert-butyl alcohol (184.4 mL, 184.4 mmol) is added slowly to a solution of chloroacetonitrile (10.8 mL, 167.6 mmol) and cyclopentanone (15.0 mL, 167.6 mmol) in anhydrous t-butyl alcohol (33 mL). The reaction is stirred at room temperature for 16 h. The mixture is filtered through diatomaceous earth, the solvent is removed, and the residue is diluted with water. The mixture is neutralized with 30% aq.sodium dihydrogen phosphate solution and extracted with diethyl ether. The organic layers are combined, dried over anhydrous sodium sulfate, filtered, and the solvent is removed. The residue is purified by flash chromatography over silica gel to obtain 14.1 g of the title compound as a colourless oil. 1H NMR (CDCl3) δ (ppm): 3.46 (s, 1H), 1.65-2.20 (m, 8H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207344B2
出典データセットuspto-grants-2012_06
ORD IDord-e58bb991c90d4e9fba888f668681538f
出典メモuspto-grants-2012_06