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HRID 5344作成日:2026年10月23日

Water → 2-Oxo-3-carboethoxy-4-(2-bromo-5-methoxyphenyl)butanoic acid, ethyl ester

https://huagongshe.com/ja/reaction/5344

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Diethyl EtherHCID 3283—
反応物Diethyl OxalateHCID 7268—
反応物Potassium tert-butoxideHCID 23665647—
反応物2-Bromo-5-methoxyphenyl-propionateHCID 131718119—
生成物2-Oxo-3-carboethoxy-4-(2-bromo-5-methoxyphenyl)butanoic acid, ethyl esterHCID 1566234090%

反応条件

温度0 °C

反応手順

Potassium t-butoxide (6.72 g) was suspended in 30 ml of anhydrous ether and cooled to 0° C. A solution of 14.35 g of ethyl 3-(2-bromo-5-methoxyphenyl-propionate and 10.95 g diethyl oxalate in 10 ml ether was added dropwise over 15 min. After 2 at 25° C., the reaction was poured into 100 ml H2O and the aqueous layer was separated, acidified to pH 1 and extracted with ether. The ether layer was dried (MgSO4) and the solvent was evaporated to yield 17.48 g of the desired product as a colorless oil (90%). NMR (CDCl3) δ1.20 (t, 3H), 1.35 (t, 3H), 3.32 (dd, 2H), 3.76 (s, 3H), 4.18 (q, 2H), 4.32 (q, 2H), 4.53 (t, 1H), 6.67 (dd, 1H), 6.80 (d, 1H), 7.40 (d, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05244888
出典データセットuspto-grants-1993_09
ORD IDord-29b1539b5e8e4303be8267bfa4999d0d
出典メモuspto-grants-1993_09