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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1730688생성일: 2026년 10월 27일

Methacrylic Acid → 4-Hydroxybutyl methacrylate

https://huagongshe.com/reaction/1730688

반응식

참여 물질

역할이름HCID투입량
반응물Methacrylic AcidHCID 4093—
반응물1,2-EpoxybutaneHCID 7834—
반응물Benzyltrimethylammonium methoxideHCID 8504—
반응물Sodium HydroxideHCID 14798—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물4-Hydroxybutyl methacrylateHCID 7045751.9%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03993684
출처 데이터셋uspto-grants-1976_11
ORD IDord-6f31e2adb0e645619c8b5d7e73fb5d8c
출처 메모uspto-grants-1976_11