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HRID 497415作成日:2026年10月27日

Ethyl bromoacetate → Acetic acid, (p-tolylsulfonyl)-, ethyl ester

https://huagongshe.com/reaction/497415

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromoacetateHCID 7748—
反応物Potassium CarbonateHCID 11430—
反応物6-Methoxy-3-nitro-2-(toluene-4-sulfonylmethyl)-pyridineHCID 13626514—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物Acetic acid, (p-tolylsulfonyl)-, ethyl esterHCID 76102—

反応条件

温度50 °C

反応手順

A mixture of 5.0 g (15.5 mmol) of 6-methoxy-3-nitro-2-(toluene-4-sulfonyl methyl)-pyridine and 1.8 mL (16 mmol) of ethyl bromoacetate is dissolved in 20 mL of DMF. To this solution is added 4.4 g (32 mmol) of K2CO3 and the reaction mixture is heated to 50° C. for 18 hours. The reaction mixture is cooled to room temperature and diluted with 300 mL of water. The mixture is extracted with ethyl acetate. The ethyl acetate extracts are dried (Na2SO4) and evaporated to yield 7.2 grams of 6-methoxy-3-nitro-pyridin-2-yl]-[toluene-4-sulfonyl]-acetic acid ethyl ester. 1H NMR (CDCl3) δ 8.30 (d, 1H), 7.60 (d, 2H), 7.30 (d, 2H), 6.80 (d, 1H), 6.30 (m, 1H), 4.0 (q, 2H), 3.80 (s, 3H), 3.60 (m, 1H), 3.10 (m, 1H), 2.40 (s, 3H), 1.10 (t, 3H). Mass spectrum: m/e=409.0 (p+1). TLC (7/3: hexanes/ethyl acetate) Rf=0.5. Step 3:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06949562B2
出典データセットuspto-grants-2005_09
ORD IDord-cb271b46556548aebf195e13a84d822a
出典メモuspto-grants-2005_09