돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2374719생성일: 2026년 10월 26일

Hydrochloric Acid → 4-[2-(2-Chlorobenzoylamino)benzoylamino]butanoic acid

https://huagongshe.com/reaction/2374719

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물ChlorotrimethylsilaneHCID 6397—
반응물TriethylamineHCID 8471—
반응물Sodium HydroxideHCID 14798—
반응물2-Chlorobenzoyl chlorideHCID 69110—
반응물4-(2-Aminobenzamido)butanoic acidHCID 13442375—
용매DichloromethaneHCID 6344—
생성물4-[2-(2-Chlorobenzoylamino)benzoylamino]butanoic acidHCID 23118564—

반응 단계

To a suspension of 2.00 g (9.01 mmol) of 4-(2-aminobenzoylamino)butanoic acid in 20 mL of dry methylene chloride, add 8.36 g (77.00 mmol) of trimethylsilyl chloride and allow the reaction to reflux for 5 hours. Then place the flask in an ice bath and add 1.17 g (11.55 mmol) of triethylamine and a solution of 1.35 g (7.70 mmol) of 2-chlorobenzoyl chloride dissolved in 5 mL of dry methylene chloride. Allow the reaction to stir for 30 minutes in an ice bath and 24 hours at room temperature. Eliminate the solvent at low pressure, add 30 ml of 10% NaOH to the crude product and continue stirring the mixture until the oil has completely disappeared. Immediately acidify with concentrated HCl and extract several times with ethyl acetate. Dry the organic phase with MgSO4 anhydrous and eliminate at low pressure. Wash the crude product several times with ether and finally, purify by recrystallization (EtOH/H2O). This yields 1.27 g (36%) of 4-[2-(2-chlorobenzoylamino)benzoylamino]butanoic acid as a brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07462735B2
출처 데이터셋uspto-grants-2008_12
ORD IDord-deb66748c80c4cb08482d6a424814c9e
출처 메모uspto-grants-2008_12