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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42848생성일: 2026년 10월 25일

Nitrogen → Ethyl 2-formyl-1,3-oxazole-4-carboxylate

https://huagongshe.com/reaction/42848

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물WaterHCID 962—
반응물ethyl 2-[(E)-2-phenylethenyl]-1,3-oxazole-4-carboxylateHCID 5708074—
용매AcetoneHCID 180—
생성물Ethyl 2-formyl-1,3-oxazole-4-carboxylateHCID 10583255—

반응 단계

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of Na104 (3.21 g, 15.00 mmol) in water (26.0) mL was slowly added to a vigorously stirred suspension of silica gel (15.0 g) in acetone (60.0 mL). The mixture was then concentrated under reduced pressure and the lumpy solid slurried in CH2Cl2 and the solvent was evaporated under reduced pressure. CH2Cl2 (40.0 mL) was added and the reaction mixture was treated at rt with (E)-2-styryl-oxazole-4-carboxylic acid ethyl ester (1.22 g, 5.00 mmol) and RuCl3 hydrate (82 mg, 0.15 mmol). The reaction mixture was stirred at rt in the dark for 30 min, filtered and concentrated under reduced pressure. Purification of the residue by FC (1:9 to 1:2 EA-Hept) gave the title compound as a yellow solid. TLC:rf (3:2 EA-Hept)=0.21. LC-MS-conditions 02: tR=0.51 min; [M+H2O+H]+=188.50.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536209B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-0271fb335694472fac8c6566c4791fa0
출처 메모uspto-grants-2013_09