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HRID 1289020作成日:2026年10月25日

Butyl methyl ether → HCID 18925346、化合物

https://huagongshe.com/reaction/1289020

反応式

関与物質

役割名称HCID仕込み量
反応物Butyl methyl etherHCID 12338—
反応物Butanoic acid, 2-bromo-, ethyl esterHCID 79039—
反応物Sodium MethoxideHCID 10942334—
反応物3-(2-Benzyloxyethoxy)-4-methoxy-benzaldehydeHCID 21716329—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物HCID 18925346HCID 18925346—

反応手順

24 g of the product of step (ii) 21.5 g bromobutyric acid ethyl ester and 30 ml t.butyl methyl ether are added dropwise over 50 mins. at 5° C. to a pre-prepared suspension of sodium methylate in 25 ml t.butyl methyl ether. The reaction mixture is stirred for 45 mins. at ca. 5° C. and then stirred for 12 hrs. at room temperature. The pH is adjusted to 5 by addition of glacial acetic acid and the obtained suspension diluted with H2O and extracted 3× with t.butyl methyl ether. The organic phase is extracted with NaHCO3 (1×) and brine (1×), and evaporated to ca. 100 ml. 13.5 ml 50% aqueous NaOH are added drop-wise and the whole stirred for 2 hrs. at 40° C., diluted with 50 ml. H2O and stirred for a further 30 mins. at room temperature. The organic phase is separated and the aqueous phase adjusted to pH 1 at max. 40° C. with 15 ml conc. HCl. The reaction mixture is stirred at 40° C. for a further 1.5 hrs., cooled to room temperature and extracted with toluene. The organic phase is washed with NaHCO3 and brine, dried over Na2SO4, filtered and evaporated to yield the title compound as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05747506
出典データセットuspto-grants-1998_05
ORD IDord-65e29963b8bb4ab7b552258883b5b431
出典メモuspto-grants-1998_05