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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 85383생성일: 2026년 10월 24일

Salicylic Acid → Benzyl 3-(2-hydroxybenzamido)butan-2-ylcarbamate

https://huagongshe.com/ko/reaction/85383

반응식

참여 물질

역할이름HCID투입량
반응물Salicylic AcidHCID 338—
반응물ImidazoleHCID 795—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물Benzyl 3-aminobutan-2-ylcarbamateHCID 59193262—
용매Ethyl AcetateHCID 8857—
생성물Benzyl 3-(2-hydroxybenzamido)butan-2-ylcarbamateHCID 6717490240%

반응 단계

To a mixture of benzyl 3-aminobutan-2-ylcarbamate (5.3 g, 23.8 mmol), 2-hydroxybenzoic acid (3.28 g, 23.8 mmol) and imidazole (1.62 g, 23.8 mmol) in EtOAc (180 mL) at 0° C. was slowly added a solution of DCC (4.90 g, 23.8 mmol) in EtOAc (20 mL). The reaction mixture was stirred (RT, 16 h), filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel, eluting with PE-EtOAc (5:1) to afford benzyl 3-(2-hydroxybenzamido)butan-2-ylcarbamate (3.2 g, 40%) as a colorless oil. Mass calculated for C19H22N2O4=342.39; found: [M+H]+=343.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846972B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-38642b5744a5467297104ac57dccd354
출처 메모uspto-grants-2014_09