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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36060생성일: 2026년 10월 24일

Hydrochloric Acid → Furaneol

https://huagongshe.com/ko/reaction/36060

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Diethyl OxalateHCID 7268—
반응물Sodium HydroxideHCID 14798—
반응물tert-Butyl methyl etherHCID 15413—
반응물Sodium MethoxideHCID 10942334—
생성물FuraneolHCID 1930974.2%

반응 단계

To a suspension of 113.4 g of sodium methylate in 750 g of methyl t-butyl ether was added at 5° C. in one hour 146 g of diethyl oxalate followed by a stirring period of one hour at 5° C. Then 204 g of diethyl 2-methyldiglycolate in two hours was added at 5° C. and the mixture was stirred for four hours at that temperature followed by a reflux period of three hours. The reaction mixture was added to 797 g of 8.9% hydrochloric acid solution at 20° C. and the pH of the resulting mixture was adjusted to 5 with 33% sodium hydroxide solution. To the separated upper layer was added with stirring 903 g of 17.8% sodium hydroxide solution at 20° C. The layers were allowed to settle and the separated lower layer was kept at 20° C. for 20 hours. Then, 200 g of water was added, 104 g of methyl bromide was introduced at 20° C. in one hour, and the mixture was stirred for another hour; and the pH of the solution was adjusted to 6.5 by the addition of concentrated hydrochloric acid solution. Extraction with methyl t-butyl ether yielded 95 g of 2,5-dimethyl-4-hydroxy-3[2H] furanone of 97.3% purity (molar overall yield 72.2%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05412121
출처 데이터셋uspto-grants-1995_05
ORD IDord-58efa3bdb6a3488f8c51b19354e7aa37
출처 메모uspto-grants-1995_05