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HRID 458500作成日:2026年10月26日

Tyrosol → Tert-butyl [4-(2-hydroxyethyl)phenoxy]acetate

https://huagongshe.com/reaction/458500

反応式

関与物質

役割名称HCID仕込み量
反応物TyrosolHCID 10393—
反応物Potassium CarbonateHCID 11430—
反応物tert-Butyl bromoacetateHCID 79177—
溶媒AcetonitrileHCID 6342—
生成物Tert-butyl [4-(2-hydroxyethyl)phenoxy]acetateHCID 23119602—

反応手順

The hapten p-(carboxymethyl)ritodrine (Hapten E) was prepared in four steps according to FIG. 7 of the accompanying drawings, from 2-(4-hydroxyphenyl)ethanol 17. The reaction of 17 with t-butyl bromoacetate in acetonitrile in the presence of potassium carbonate at 60° C. gives 2-[4-(t-butoxycarbonylmethoxy)phenyl]ethanol 18. The oxidation of the alcohol 18 with pyridinium chlorochromate (pcc) in dichloromethane gives the 2-[4-(t-butoxycarbonylmethoxy)phenyl]ethanal 19. The ester 20, obtained by condensation of the aldehyde 19 with α-(1-aminoethyl)-4-hydroxybenzyl alcohol hydrochloride 13 in methanol in the presence of sodium cyanoborohydride and triethylamine. Deprotection of the t-butyl protecting group of the ester 20 with 4 M HCl in dioxane at room temperature gave Hapten E in moderate yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07192722B2
出典データセットuspto-grants-2007_03
ORD IDord-840cea4db1a04a7d8d622476971a7924
出典メモuspto-grants-2007_03