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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16967생성일: 2026년 10월 23일

4-Methoxybenzyl alcohol → ethyl 2-((N-(butyloxycarbonyl)-N-(p-methoxybenzyl)sulfamoyl)amino)acetate

https://huagongshe.com/ko/reaction/16967

반응식

참여 물질

역할이름HCID투입량
반응물4-Methoxybenzyl alcoholHCID 7738—
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl azodicarboxylateHCID 5363146—
반응물ethyl 2-((N-(butyloxycarbonyl)sulfamoyl)amino)acetateHCID 18449914—
용매TetrahydrofuranHCID 8028—
생성물ethyl 2-((N-(butyloxycarbonyl)-N-(p-methoxybenzyl)sulfamoyl)amino)acetateHCID 1844991369%

반응 조건

온도0 °C

반응 단계

To a solution of (4-methoxyphenyl)-methanol (1.4 g, 8.5 mmol) and triphenyl-phosphane (2.6 g, 8.5 mol) in dry THF was added a solution of ethyl 2-((N-(butyloxycarbonyl)sulfamoyl)amino)acetate from the previous step (2.4 g, 8.5 mol) and DIAD (2.0 g, 8.5 mmol) in dry THF dropwise at 0° C. under N2 atmosphere. The mixture was stirred at 0° C. for 2 h, warmed to RT and stirred overnight. After the solvent was removed in vacuo, the residue was purified by column chromatography to afford ethyl 2-((N-(butyloxycarbonyl)-N-(p-methoxybenzyl)sulfamoyl)amino)acetate (2.3 g, 69%) as a white solid. 1H-NMR (CDCl3): δ 7.32 (d, J=8.8 Hz, 2H), 6.85 (d, J=8.8 Hz, 2H), 5.71 (m, 1H), 4.76 (s, 2H), 4.14 (q, J=7.2 Hz, 2H), 3.80 (s, 3H), 3.55 (d, J=5.2 Hz, 2H), 1.54 (s, 9H), 1.25 (t, J=7.2 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737283B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-32ec822684a44ab987aa9823d61c5656
출처 메모uspto-grants-2010_06