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HRID 1648035作成日:2026年10月27日

Triphenylphosphine → 2-[(5-Hexynyl)oxy]benzenepropanoic acid methyl ester

https://huagongshe.com/reaction/1648035

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物5-Hexyn-1-olHCID 70234—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物Methyl 3-(2-hydroxyphenyl)propionateHCID 2794569—
溶媒TetrahydrofuranHCID 8028—
生成物2-[(5-Hexynyl)oxy]benzenepropanoic acid methyl esterHCID 5378944877%

反応手順

A mixture of 0.98 g (10 mmol) of 5-hexyn-1-ol, 1.98 g (11 mmol) of 2-hydroxybenzenepropanoic acid methyl ester, 2.88 g (11 mmol) of triphenylphosphine, 1.91 g (11 mmol) of diethyl azodicarboxylate, and 220 mL of dry tetrahydrofuran was stirred at room temperature for 100 hr and then concentrated under reduced pressure. The residue was triturated with 9:1 hexane-ether. The solid was filtered with suction and washed with the same solvent mixture. The filtrate and washes were combined and concentrated in vacuo. Flash chromatography of the residue on silica gel, eluting with 9:1 hexane-ether gave 2 g (77%) of 2-[(5-hexynyl)oxy]benzenepropanoic acid methyl ester as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05434186
出典データセットuspto-grants-1995_07
ORD IDord-ca4921c997bc4acaa14a72107dae2424
出典メモuspto-grants-1995_07