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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72076생성일: 2026년 10월 23일

Ammonium Chloride → HCID 21879615, 화합물

https://huagongshe.com/ko/reaction/72076

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물6-Bromo-2-naphthalenecarboxylic acidHCID 4549852—
반응물5,6-Dihydropyrrolo[1,2-c]imidazol-7-oneHCID 11170960—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
용매Ethyl AcetateHCID 8857—
생성물HCID 21879615HCID 2187961512.2%

반응 조건

온도-100 °C

반응 단계

6-Bromo-2-naphthoic acid (1.51 g) was dissolved in dry THF (50 ml), and cooled to −100° C. in a liquid nitrogen/diethyl ether bath. Under stirring a solution (1.6M; 7.88 ml) of n-butyllithium in hexane was added dropwise at −95° C. or below over 5 min. After stirring at −100° C. for 30 min and at −80° C. for 10 min, the mixture was cooled to −100° C. again. A solution of 5,6-dihydro-7H-pyrrolo[1,2-c]imidazol-7-one (0.61 g) in dry THF (11 ml) was added dropwise at −90° C. or below over 5 min. After stirring at the same temperature for 30 min, the temperature was raised to −70° C. over 30 min, and saturated aqueous ammonium chloride solution (25 ml) was added to quench the reaction. After stirring for 10 min, ethyl acetate (50 ml) was added to partition the solution. The organic layer was removed and the aqueous layer was concentrated to dryness. The obtained residue was purified by flash column chromatography, and the object fraction was dissolved in methanol. This solution was concentrated, ether was added to the precipitated powder and the powder was collected by filtration and dried. The title compound (180 mg) was obtained as a colorless powder. The mother liquor was concentrated to give a residue (449 mg) containing the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828429B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-eee504e596d047aa96630c28e07c86e5
출처 메모uspto-grants-2014_09