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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52881생성일: 2026년 10월 24일

Ethyl Acetate → Pivaloyloxymethyl 1-[(2'-t-butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-4-hydroxymethylimidazole-5-carboxylate

https://huagongshe.com/ko/reaction/52881

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Potassium CarbonateHCID 11430—
반응물Chloromethyl pivalateHCID 87885—
반응물1-[(2'-t-Butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-4-hydroxymethylimidazole-5-carboxylic acidHCID 19036119—
용매WaterHCID 962—
용매DimethylacetamideHCID 31374—
생성물Pivaloyloxymethyl 1-[(2'-t-butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-4-hydroxymethylimidazole-5-carboxylateHCID 1903618190.2%

반응 단계

350 mg of potassium carbonate were added to a solution of 552 mg of 1-[(2'-t-butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-4-hydroxymethylimidazole-5-carboxylic acid (prepared as described in Example 4) and 220 mg of pivaloyloxymethyl chloride in 7 ml of N,N-dimethylacetamide, and the resulting mixture was stirred at room temperature for 5 hours. At the end of this time, the reaction mixture was mixed with ethyl acetate and water, and the ethyl acetate layer was separated and dried over anhydrous magnesium sulfate; the solvent was then removed by distillation under reduced pressure. The resulting residue was purified by column chromatography through silica gel, using ethyl acetate as the eluent, to give 0.62 g of the title compound as a syrup.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616599
출처 데이터셋uspto-grants-1997_04
ORD IDord-b64c46f517f34819a0036b46f94e10df
출처 메모uspto-grants-1997_04