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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 726719생성일: 2026년 10월 26일

Hydrochloric Acid → 3-[4-Cyanobenzyl]aminopropanoic acid

https://huagongshe.com/reaction/726719

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-CyanobenzaldehydeHCID 66042—
반응물Ethyl 3-aminopropanoateHCID 419889—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물Lithium hydroxide methanolHCID 23717829—
용매Acetic AcidHCID 176—
용매DimethylformamideHCID 6228—
생성물3-[4-Cyanobenzyl]aminopropanoic acidHCID 1676998779%

반응 단계

4-cyanobenzaldehyde (0.65 g; 5 mmoles) and β-alanine ethyl ester.HCl (0.76 g; 5 mmoles) were dissolved in N,N-dimethylformamide (10 ml) containing 1% acetic acid. After 10 min., sodiumcyanoborohydride (0.35 g; 5 mmoles) was added to the solution. The reaction mixture was stirred at room temperature for 12 hrs. and taken down to dryness under reduced pressure. The residue was treated with 1N lithium hydroxide/methanol (1:1; 20 ml) for 15 min. Methanol was removed and the pH of the remaining solution was adjusted to pH 5 with 50% acetic acid. The product was purified by HPLC using a linear gradient of acetonitrile/water/trifluoroacetic acid. The desired fractions was collected and lyophilized to give 0.81 g of white solid (79% yield). FAB-MS: MH+ =205.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05710166
출처 데이터셋uspto-grants-1998_01
ORD IDord-c6ad0981756643088329bfd4623ad976
출처 메모uspto-grants-1998_01