戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 655078作成日:2026年10月26日

Lilial → (E)-3(2-Hydroxy-phenyl)-acrylic acid 3(4-tert-butyl-phenyl)-1-ethoxy-propyl ester

https://huagongshe.com/reaction/655078

反応式

関与物質

役割名称HCID仕込み量
反応物LilialHCID 228987—
反応物(E)-3-[2(tert-Butyl-dimethyl-silanoxy)-phenyl]-acrylic acidHCID 22290462—
反応物1-Tert-butyl-4-(3-ethoxy-2-methyl-allyl)-benzeneHCID 54077483—
触媒p-Toluenesulfonic acidHCID 6101—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物(E)-3(2-Hydroxy-phenyl)-acrylic acid 3(4-tert-butyl-phenyl)-1-ethoxy-propyl esterHCID 6852321528.2%

反応手順

A solution of 3.1 g of (E)-3-[2-(tert-Butyl-dimethyl-silanoxy)-phenyl]-acrylic acid, 3.0 g of 1-tert-butyl-4-(3-ethoxy-2-methyl-allyl)-benzene, accessible from 3-(4-tert-butyl-phenyl)-2-methyl-propionaldehyde via a two step procedure according to P. D. Bartlett and A A. Frimer, Heterocycles 11, 419-435, (1978), and 20 mg of p-TSA in 25 ml of toluene was stirred at 0° C. for 4 h and at room temperature for 14 h. The reaction mixture was partitioned between saturated sodium carbonate and hexane and the organic layer was washed with brine, dried over (Na2SO4) and evaporated to dryness to yield 5.3 g of the crude intermediate (E)-3-[2-(tert-Butyl-dimethyl-silanoxy)-phenyl]-acrylic acid 3-(4-tert-butyl-phenyl)-1-ethoxy-propyl ester as a pale yellow oil. This was dissolved in 20 ml of THF and treated at 0° C. with 3.2 g of solid TBAF-3H2O. After 30 min., the mixture was concentrated and purification by repeated flash chromatography yielded 1.2 g of the title ester (a mixture of diastereoisomers) as a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE043006E1
出典データセットuspto-grants-2011_12
ORD IDord-5fc8dd8969f5410f93583b2e57cc2393
出典メモuspto-grants-2011_12