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HRID 1730688作成日:2026年10月27日

Methacrylic Acid → 4-Hydroxybutyl methacrylate

https://huagongshe.com/reaction/1730688

反応式

関与物質

役割名称HCID仕込み量
反応物Methacrylic AcidHCID 4093—
反応物1,2-EpoxybutaneHCID 7834—
反応物Benzyltrimethylammonium methoxideHCID 8504—
反応物Sodium HydroxideHCID 14798—
溶媒MethanolHCID 887—
溶媒Ethyl AcetateHCID 8857—
生成物4-Hydroxybutyl methacrylateHCID 7045751.9%

反応手順

Methacrylic acid (86 g.), 1,2-epoxybutane (36 g.), and a 40% solution of benzyltrimethylammoniummethoxide in methanol (21 g.) were charged to a round bottom flask and stirred at room temperature for 98 hours. 300 ml. of a 7% sodium hydroxide solution and 200 ml. of ethyl acetate were added to the mixture, the organic layer separated, and the basic aqueous layer given a second wash with 200 ml. of ethyl acetate. The organic fractions were then combined, and washed successively with 300 ml. of 7% sodium hydroxide and three 200 ml. portions of water, the spent wash solutions being decanted between washings. Excess moisture was removed from the washed organic phase with sodium sulfate and the ethyl acetate was stripped off to yield hydroxybutyl methacrylate (41 g.). This product was taken up in 60 ml. of benzene and pyridine (22 g.). Cinnamoyl chloride (50.4 g.) in 75 ml. of benzene was added dropwise with stirring to the hydroxybutyl methacrylate solution and the resulting mixture allowed to react for a period of 24 hours. After the reaction was complete pyridine hydrochloride formed by the reaction was filtered off, the filtrate washed and the product cinnamoylated hydroxybutyl methacrylate recovered in the manner described in Example 8.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03993684
出典データセットuspto-grants-1976_11
ORD IDord-6f31e2adb0e645619c8b5d7e73fb5d8c
出典メモuspto-grants-1976_11