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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83813생성일: 2026년 10월 24일

Dicyclohexylcarbodiimide → 4-(2-Benzyloxyacetylamino)phenoxyacetic acid methyl ester

https://huagongshe.com/ko/reaction/83813

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물(Benzyloxy)acetic acidHCID 290301—
반응물Methyl(4-aminophenoxy)acetateHCID 6422115—
용매DichloromethaneHCID 6344—
생성물4-(2-Benzyloxyacetylamino)phenoxyacetic acid methyl esterHCID 5925398368.9%

반응 단계

To a mixture of (4-aminophenoxy)-acetic acid methyl ester 3 (20 g, 110.5 mmol) and benzyloxy acetic acid (20.4 g, 123 mmol) in anhydrous dichloromethane (200 ml) under nitrogen atmosphere was added dropwise a solution of 1,3-dicyclohexyl carbo-diimide (63.2 g, 306 mmol) in anhydrous dichloromethane (80 ml) then stirred at room temp. for 12 hours. The solids were filtered off, the dichloromethane was washed with 5% sodium bicarbonate solution (100 ml), water (100 ml) added, and the solids dried over sodium sulphate and distilled to get crude 49. Crude 49 was purified by column chromatography on silica gel using benzene as eluant to get pure 49 (25 g, 68.9%) as a white powder with an m.p. between 76-77.5° C. 1H NMR (CDCl3) δ 3.82 (s, 3H, ester), 4.10 (s, 2H, CH2), 4.62 (s, 2H, CH2), 4.66 (s, 2H, CH2), 6.88 (d, 2H, Ar), 7.38 (m, 5H, Ar), 7.46 (d, 2H, Ar), 8.24 (bs, 1H, NH)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846845B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-c57186fa43784b8e8a50548a6a12cdb3
출처 메모uspto-grants-2014_09