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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 444976생성일: 2026년 10월 24일

4-Formylbenzoic acid → 4-[(2-tert-Butoxycarbonylethylamino)methyl]benzoic acid

https://huagongshe.com/ko/reaction/444976

반응식

참여 물질

역할이름HCID투입량
반응물4-Formylbenzoic acidHCID 12088—
반응물DiisopropylethylamineHCID 81531—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물Tert-butyl 3-aminopropanoate hydrochlorideHCID 16218890—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물4-[(2-tert-Butoxycarbonylethylamino)methyl]benzoic acidHCID 59687909—

반응 단계

Tert-butyl 3-aminopropanoate hydrochloride (5 g, 27.7 mmol) was dissolved in methanol (150 mL). Diisopropylethylamin (4.73 mL, 27.7 mmol) was added followed by 4-carboxybenzaldehyd. The mixture is heated to reflux for 1 hour. After cooling to room temperature sodium cyanoborohydride (1.77 g, 22.1 mmol) was added under nitrogen and stirred for 1 hour at room temperature. Acetic acid (15 mL) was added and the mixture was stirred for an additional 1 hour. The mixture was poured into water (300 mL) and stirred at room temperature over night. The water solution was washed with ethyl acetate (3×250 mL). The organic phase dried (Na2SO4) and solvent removed in vacuo to yield the crude product as an oil which solidifies by standing. The crude product was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08476228B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-529bb2850dd94b4484bee76555c5f515
출처 메모uspto-grants-2013_07