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HRID 463340作成日:2026年10月25日

Triphenylphosphine → Ethyl [5-{5-(4-methoxy-3-propylphenyl)pentyloxy}-1-naphthalenyloxy]acetate

https://huagongshe.com/reaction/463340

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5-(4-Methoxy-3-propylphenyl)pentanolHCID 20282931—
反応物Ethyl(5-hydroxy-1-naphthalenyloxy)acetateHCID 20475151—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl [5-{5-(4-methoxy-3-propylphenyl)pentyloxy}-1-naphthalenyloxy]acetateHCID 5457478279.5%

反応手順

To a stirred suspension of 5-(4-methoxy-3-propylphenyl)pentanol (2.48 g), ethyl (5-hydroxy-1-naphthalenyloxy)acetate (2 g), and triphenylphosphine (3.2 g) in dry tetrahydrofuran (30 ml) under nitrogen was added diethyl azodicarboxylate (1.65 ml) slowly so that the temperature did not rise above 50°. After 3 hours the solution was evaporated, and the residue was chromatographed on silica with a mixture of dichloromethane and light petroleum (bp 40°-60°) (4:6) to give the sub-title ester (3 g), mp 70° (from ethanol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04518612
出典データセットuspto-grants-1985_05
ORD IDord-ebc4e97402b44fd087f7b97509c1aa7e
出典メモuspto-grants-1985_05