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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1728953생성일: 2026년 10월 26일

Hydrochloric Acid → HCID 178470333, 화합물

https://huagongshe.com/reaction/1728953

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium ChlorideHCID 5234—
반응물Diethyl OxalateHCID 7268—
반응물Potassium thiocyanateHCID 516872—
반응물SodiumHCID 5360545—
반응물ethyl 2-(N-phenylformamido)acetateHCID 14416604—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물HCID 178470333HCID 17847033348%

반응 단계

Absolute ethanol (50 mL) was slowly added to a mechanically stirred suspension of finely cut sodium metal (19.3 g; 0.84 mol) in anhydrous ether (500 mL). When most of the metal had dissolved, diethyl oxalate (114 mL; 0.84 mol) was slowly added followed by the slow addition of the N-phenyl-N-formylglycine ethyl ester (130 g; 0.67 mol). The mixture was stirred at room temperature overnight and then ice-water (700 mL) was added. The resulting emulsion was broken by sequential addition of a saturated sodium chloride solution (150 mL) and water (200 mL). The aqueous layer was removed, potassium thiocyanate (114 g; 1.18 mol) was added, then concentrated hydrochloric acid (160 mL), followed by absolute ethanol (900 mL). The resultant mixture was warmed at 60°-65° C. for 1 hour, then at 50° C. for 6 hours and finally allowed to stir at room temperature overnight. The light yellow precipitate was filtered, washed with ethanol and dried to give 103 g (48%) of diethyl 2-mercapto-1-phenyl-4,5-imidazoledicarboxylate (mp 145°-146° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05329012
출처 데이터셋uspto-grants-1994_07
ORD IDord-1706884c5fd742b48f17201e467f3009
출처 메모uspto-grants-1994_07