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HRID 718555作成日:2026年10月26日

Acetic Acid → 5-(4-(4-tert-Butylphenyl)-3-methylbut-1-enyl)benzo[d][1,3]dioxole

https://huagongshe.com/reaction/718555

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物LilialHCID 228987—
反応物(Benzo[d][1,3]dioxol-5-ylmethyl)triphenylphosphonium bromideHCID 10695955—
溶媒TetrahydrofuranHCID 8028—
生成物5-(4-(4-tert-Butylphenyl)-3-methylbut-1-enyl)benzo[d][1,3]dioxoleHCID 8670279188%

反応条件

温度25 °C

反応手順

Potassium t-butylat (1 Min THF, 11 mL, 11.0 mmol, 1.1 equiv.) was added to a solution of (benzo[d][1,3]dioxol-5-ylmethyl)triphenylphosphonium bromide (4.77 g, 10.0 mmol, 1.0 equiv.) in THF (20 mL) at 25° C. After the dark red suspension was stirred at 25° C. for 10 min, 3-(4-tert-butylphenyl)-2-methylpropanal (2.04 g, 10.0 mmol, 1.0 equiv.) in THF (10 mL) was added, and the mixture was stirred at 70° C. for 1.5 h. After addition of 20% aq. AcOH-solution (10 mL) at 25° C., the aqueous layer was extracted with hexanes, the combined organic phases were dried (MgSO4), filtered and the filtrate was concentrated. The residue was purified by flash chromatography on SiO2 (hexanes/EtOAc 19:1) to yield 2.83 g (88%) of the title compound as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09193935B2
出典データセットuspto-grants-2015_11
ORD IDord-7c534bb7fff64b7e84363882a9867388
出典メモuspto-grants-2015_11