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HRID 1250800作成日:2026年10月25日

Triphenylphosphine → 4-(6-Hydroxyhexyloxy)-3-methoxycinnamic acid methyl ester

https://huagongshe.com/reaction/1250800

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物Methyl FerulateHCID 5357283—
反応物6-(Ethenyloxy)-1-hexanolHCID 22026199—
触媒Sulfuric AcidHCID 1118—
溶媒MethanolHCID 887—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物4-(6-Hydroxyhexyloxy)-3-methoxycinnamic acid methyl esterHCID 5414706282.8%

反応条件

温度0 °C

反応手順

3.92 ml (25.2 mmol) of 1,6-hexanediol vinyl ether were added to a solution of 5.0 g (24.0 mmol) of (E)-4-hydroxy-3-methoxycinnamic acid methyl ester and 6.61 g (25.2 mmol) of triphenylphosphine in 150 ml of tetrahydrofuran. The colourless solution was subsequently cooled to 0° C. and then 11.5 ml (25.3 mmol) of a 40% solution of azodicarboxylic acid diethyl ester in toluene were added dropwise thereto in the course of 30 minutes. The mixture was subsequently allowed to react first for 30 minutes at 0° C. and then for 22.5 hours at room temperature. 150 ml of methanol and 10 drops of concentrated sulphuric acid were then added to the reaction solution and the mixture was stirred for 1.5 hours. The reaction mixture was then partitioned between ethyl acetate and water; the organic phase was washed with a saturated sodium bicarbonate solution and repeatedly with saturated sodium chloride solution, dried over magnesium sulphate, filtered and concentrated by evaporation. Chromatography of the residue on 470 g of silica gel using toluene/ethyl acetate 1:1 and subsequent crystallisation from ethyl acetate/hexane 3:5 yielded 6.13 g of 4-(6-hydroxyhexyloxy)-3-methoxycinnamic acid methyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06340506B1
出典データセットuspto-grants-2002_01
ORD IDord-fdfd1fd62e9d40e9aaec8bbe69797535
出典メモuspto-grants-2002_01