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HRID 268693作成日:2026年10月25日

2-Ethylhexyl methacrylate → 3-Ethoxy-4-hydroxymandelic acid

https://huagongshe.com/reaction/268693

反応式

関与物質

役割名称HCID仕込み量
反応物2-Ethylhexyl methacrylateHCID 12713—
反応物4-MethoxybenzaldehydeHCID 31244—
反応物Silane, ((1-methoxy-2-methyl-1-propenyl)oxy)trimethyl-HCID 552336—
反応物2-Propenoic acid, 2-methyl-, trimethylsilyl esterHCID 2733839—
触媒HCID 68463681HCID 68463681—
溶媒MethanolHCID 887—
溶媒AcetonitrileHCID 6342—
溶媒TetrahydrofuranHCID 8028—
生成物3-Ethoxy-4-hydroxymandelic acidHCID 193792—

反応手順

7 ml of THF and 16 ml of dimethylketene methyltrimethylsilylacetal as an initiator were mixed under an argon gas atmosphere, and stirred for 30 minutes. 0.64 g of tetrabutylammonium m-chlorobenzene catalyst dissolved in 1 ml of acetonitrile was added, and the mixture was stirred for 2 hours. 53.1 ml of trimethylsilyl methacrylate and 4.9 ml of 2-ethylhexyl methacrylate dissolved in 10 ml of THF were added in droplets. After performing the reaction for 2 hours, 9.8 ml of 2-ethylhexyl methacrylate dissolved in 5 ml of THF was added slowly. After performing the reaction for 3 hours, 7.6 g of 4-methoxybenzaldehyde were added to substitute the terminal end of the hydrophobic moiety. After stirring for 12 hours, 120 ml of methanol was added, heated to reflux for 6 hours, and then the solvent was removed under reduced pressures. The resulting solid was dried in a vacuum oven for 24 hours to obtain light yellow EHMA/MAA//EHMA-4-methoxylphenyl block copolymer powders.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07446135B2
出典データセットuspto-grants-2008_11
ORD IDord-36417995d64a421fbf062cb338ae4f28
出典メモuspto-grants-2008_11