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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357794생성일: 2026년 10월 25일

Sodium Thiosulfate → HCID 53710998, 화합물

https://huagongshe.com/reaction/357794

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ThiosulfateHCID 24477—
반응물Sulfuryl chlorideHCID 24648—
반응물Ethyl 2-Methyl-3-furoateHCID 261900—
용매AcetonitrileHCID 6342—
생성물HCID 53710998HCID 53710998—

반응 조건

온도10 °C

반응 단계

2-Methyl-3-furancarboxylic acid ethyl ester (10.5 g) was dissolved in acetonitrile (50 ml), and sulfuryl chloride (5.6 ml) was added under ice-cooling. The mixture was stirred at 10° C. for 30 minutes, and 10% aqueous sodium thiosulfate (100 ml) was added. The mixture was stirred at room temperature for 2 hours, and extracted with diethyl ether. The extract was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography, and the desired fractions were concentrated under reduced pressure to give 5-chloro-2-methyl-3-furancarboxylic acid ethyl ester (10 g) as oil. 5-Chloro-2-methyl-3-furancarboxylic acid ethyl ester (10 g) was dissolved in ethanol (100 ml), and 1N aqueous sodium hydroxide (60 ml) was added. The mixture was stirred under reflux for 30 minutes and concentrated under reduced pressure. The residue was dissolved in water and washed with diethyl ether. The aqueous layer was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. Precipitated crystals were recrystallized from acetone-hexane to give 5-chloro-2-methyl-3-furancarboxylic acid (5.5 g) as crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05840917
출처 데이터셋uspto-grants-1998_11
ORD IDord-98223f71e0f142808d4028278d0b7d42
출처 메모uspto-grants-1998_11