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HRID 66988作成日:2026年10月26日

Pyridine → 3-Triphenylmethoxy-1-octyne

https://huagongshe.com/reaction/66988

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物BromotriphenylmethaneHCID 11692—
反応物1-Octyn-3-olHCID 13166—
反応物Potassium BromideHCID 253877—
溶媒WaterHCID 962—
生成物3-Triphenylmethoxy-1-octyneHCID 12675347—

反応手順

A mixture of 1.26 g. (10.0 mmoles) of 1-octyn-3-ol, 4.85 g. (15.0 mmoles) of triphenylmethyl bromide, and 50 ml. of dry pyridine is heated at 95° C. for 60 minutes with occasional swirling. The solution is cooled, treated with water, and extracted with ether. The extract is washed successively with water and saturated sodium chloride solution, dried over magnesium sulfate, and concentrated. The crude product is purified by chromatography on Florisil and recrystallization from petroleum ether to give white crystals, m.p. 65°-66.5°, ν max. (KBr) 3280 (acetylenic hydrogen), 1605, 1030, and 702 cm-1 (triphenylmethoxy group).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04343949
出典データセットuspto-grants-1982_08
ORD IDord-3e964eb3d945459f83319c5b49610467
出典メモuspto-grants-1982_08