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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34424생성일: 2026년 10월 26일

Water → 2-(2-Pinanylthio)-5-(t-butylthio)-1,3,4-thiadiazole

https://huagongshe.com/reaction/34424

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물tert-ButanolHCID 6386—
반응물(+-)-alpha-PineneHCID 6654—
반응물HCID 178418558HCID 178418558—
촉매Sulfuric AcidHCID 1118—
용매O-XyleneHCID 7237—
생성물2-(2-Pinanylthio)-5-(t-butylthio)-1,3,4-thiadiazoleHCID 20129852—

반응 조건

온도140 °C

반응 단계

2,5-Dimercapto-1,3,4-thiadiazole (35 g, 0.23 mol) and alpha-pinene (35 g, 0.26 mol) were charged to a reaction vessel and heated cautiously to 140° C. (exothermic reaction). The reaction was maintained at 135°-155° C. for 15 min. The reaction was fitted with a Dean Stark trap filled with xylene. Xylene (15 ml) was charged to the reaction. The reaction was fitted with an addition funnel containing t-butanol (25 g, 0.34 mol). The alcohol was added slowly with the reaction refluxing. Sulfuric acid (3 drops) was added to accelerate the water removal. The reaction product was isolated after approximately 5 ml (about 0.25 mol) of water were collected. Solvent was stripped by rotary evaporation. The product was mixed with calcium hydroxide (1 g), hexane (about 100 ml), and sufficient acetone (about 50 ml) to maintain one liquid layer. The product was filtered using a filter aid and the solvent removed by rotary evaporation. This afforded the final product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04761482
출처 데이터셋uspto-grants-1988_08
ORD IDord-ba1ce414a207408996063908143efced
출처 메모uspto-grants-1988_08