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HRID 1721958作成日:2026年10月25日

Tetrahydrofuran → [1,1-Dimethyl-6-(2-phenylethoxy)hexyl](phenylmethyl)amino-1-[3,5-bis(phenylmethoxy)phenyl]ethanone

https://huagongshe.com/reaction/1721958

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物DiisopropylethylamineHCID 81531—
反応物1-(3,5-Bis(phenylmethoxy)phenyl)-2-bromoethan-1-oneHCID 120097—
生成物[1,1-Dimethyl-6-(2-phenylethoxy)hexyl](phenylmethyl)amino-1-[3,5-bis(phenylmethoxy)phenyl]ethanoneHCID 20029801—

反応手順

A solution of 2-bromo-1-[3,5-bis(phenylmethoxy)phenyl]ethanone (2.5 g), Intermediate 32 (2.0 g) and N,N-diisopropylethylamine (0.77 g) in THF (25 ml) was stirred at room temperature for 2 h and refluxed for 20 h. ER (100 ml) was added and the resulting suspension was filtered, the filtrate was evaporated and the residue was purified by [C] eluting with cyclohexane-ER (4:1) to give the title compound as a pale yellow oil (1.2g). T.l.c. (cyclohexane-ER 3:1) Rf 0.4

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04853381
出典データセットuspto-grants-1989_08
ORD IDord-486f7f7af5564834bf73aba0568881ec
出典メモuspto-grants-1989_08