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HRID 251783作成日:2026年10月27日

Phenol → Phenyl 3-phenylprop-2-enoate

https://huagongshe.com/reaction/251783

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物TriethylamineHCID 8471—
反応物Phenyl CinnamateHCID 785207—
反応物Cinnamoyl ChlorideHCID 5354261—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物Phenyl 3-phenylprop-2-enoateHCID 95152—

反応手順

To a 1-L three-neck flask, under a nitrogen gas stream, trans-cinnamic acid chloride (100 g, 0.60 mol), phenol (59.3 g, 0.63 mol), and THF (500 ml) were fed, and a THF solution (100 ml) of triethylamine (63.8 g, 0.63 mol) were added dropwise using a dripping funnel while being chilled with ice. After the completion of dropwise addition, 12-hour stirring was performed at room temperature, and the reaction solution was poured into water. The obtained white precipitate was filtered and dried under reduced pressure, and thereafter the yield was 135.5 g (yield rate of 99.9%). This was dissolved into approximately 200 ml of methanol by heating, and then cooled. As a result, white crystal was obtained (112.6 g, yield rate of 83.8%). Note that, the obtained crystal was confirmed to be a target trans-cinnamic acid phenyl ester by NMR structural analysis.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07867581B2
出典データセットuspto-grants-2011_01
ORD IDord-583aca9cef9f473ba95af1cb6bdb9c66
出典メモuspto-grants-2011_01