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HRID 225063作成日:2026年10月25日

Water → 4-Triphenylmethoxy-1-Octyne

https://huagongshe.com/reaction/225063

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物BromotriphenylmethaneHCID 11692—
反応物1-Octyn-4-olHCID 103656—
溶媒PyridineHCID 1049—
生成物4-Triphenylmethoxy-1-OctyneHCID 12786165—

反応手順

A mixture of 10 g (0.08 moles) of 4-hydroxy-1-octyne [1. Crombie and A. G. Jacklin, J. Chem. Soc., 1632 (1957), also Example 93] and 30.75 g (0.09 moles) of triphenylmethyl bromide in 85 ml of dry pyridine is heated on the steam bath for 2 hours. The cooled mixture is treated with water and extracted with ether. The extract is washed successively with ice cold 2% hydrochloric acid, saturated sodium chloride solution, dried with magnesium sulfate, and taken to dryness. Column chromatography of the residue on Florisil affords an oil; λ max 3.01, 4.72 (acetylenic hydrogen), 6.28, 9.65 and 14.25μ (triphenylmethoxy group).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04235797
出典データセットuspto-grants-1980_11
ORD IDord-0821d8925ff44362b629709aae0b135c
出典メモuspto-grants-1980_11