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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 493388생성일: 2026년 10월 26일

Acetic Anhydride → HCID 178482205, 화합물

https://huagongshe.com/reaction/493388

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물TriethylamineHCID 8471—
반응물Ethyl AcetateHCID 8857—
반응물HCID 178507748HCID 178507748—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물HCID 178482205HCID 178482205—

반응 단계

4-{4-[2-(phenoxymethyl)-1H-imidazol-4-yl]phenoxy}aniline (238 mg, 0.0066 mol), (prepared according to a method analogous to that described in Example 28) is suspended in dichloromethane (5 ml) at 23° C. Triethylamine (0.1 ml, 0.0079 mol) and acetic anhydride (0.062 ml, 0.0066 mol) are added. The mixture is then stirred for 20 hours then evaporated to dryness. The oil obtained is taken up with ethyl acetate and water. After decantation and extraction by ethyl acetate, the organic phase is washed with water then with a saturated solution of sodium chloride, dried over sodium sulphate then the solvent is evaporated off. The residue obtained is adsorbed on silica then purified by chromatography on a Biotage-type silica column (eluent: ethyl acetate-heptane: 7-3 to 9-1). After washing with diisopropyl ether and isopentane, a beige-coloured powder is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07534805B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-84812724710249d4b3aac5f37c78b811
출처 메모uspto-grants-2009_05