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HRID 2232262作成日:2026年10月27日

Tetradecyltrimethylammonium → 2-(4-Chlorophenyl)-3-(1H-1,2,4-triazol-1-yl)propane-1,2-diol

https://huagongshe.com/reaction/2232262

反応式

関与物質

役割名称HCID仕込み量
反応物TetradecyltrimethylammoniumHCID 14251—
反応物Sodium HydroxideHCID 14798—
反応物Sulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
反応物1-(4-Chlorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethan-1-oneHCID 716472—
溶媒TolueneHCID 1140—
生成物2-(4-Chlorophenyl)-3-(1H-1,2,4-triazol-1-yl)propane-1,2-diolHCID 13305456—

反応条件

温度60 °C

反応手順

To a stirred solution of p-chlorophenacyl-1H-1,2,4-triazole (10.3 g, 40 mmol) in 65 mL of toluene and 65 mL of 20% w/w NaOH at 60° C., add trimethylsulfoxonium iodide (8.84 g, 40 mmol) and cetrimide (0.39 g). Continue to stir the so-formed mixture at 60° C. for 1.5 h. Separate the toluene layer, add 20 mL of H2O to the aqueous layer and extract with two 100 mL portions of ethyl acetate (EtOAc). Combine both the toluene and EtOAc layers, dry oyer MgSO4, filter, and evaporate off the solvents. Add 100 mL of acetone, 6 mL of concentrated H2SO4, 20 mL of H2O, and reflux for 3 hr. Eyaporate the acetone at 45° C. under reduced pressure. Add 20 mL of sat. sodium bicarbonate and extract with two 100 mL portions of EtOAc. Wash the combined EtOAc layers with sat. brine, dry oyer MgSO 4, and evaporate the EtOAc to obtain a syrup. Chromatograph the syrup on 300 g of silica gel using 5% MeOH/CH2Cl2 as the eluent under flash chromatography conditions to obtain 3.63 g of the title product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04788190
出典データセットuspto-grants-1988_11
ORD IDord-e8ec615e92ce4b1684f68f935c9a82ac
出典メモuspto-grants-1988_11