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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 557444생성일: 2026년 10월 25일

Hydrochloric Acid → N-(2,6-Dichlorobenzoyl)-4-nitro-L-phenylalanine

https://huagongshe.com/reaction/557444

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-Nitro-3-phenyl-L-alanineHCID 13706—
반응물Sodium HydroxideHCID 14798—
반응물2,6-Dichlorobenzoyl chlorideHCID 78392—
용매AcetoneHCID 180—
용매WaterHCID 962—
생성물N-(2,6-Dichlorobenzoyl)-4-nitro-L-phenylalanineHCID 5801832295%

반응 단계

To 13 mL of acetone, there were added 10.04 g of p-nitro-L-phenylalanine and 28 mL of water to thus form a suspension and the latter was cooled in an ice-bath. To this suspension, there were alternatively dropwise added 18.4 mL of a 6M sodium hydroxide solution and 10.05 g of 2,6-dichlorobenzoyl chloride in such a manner that the pH value of the suspension was maintained at a level of not less than 13 at a temperature of not more than 15° C. After the completion of the dropwise addition, the suspension was further stirred for 2 hours with cooling in an ice-bath, then the progress of the reaction was confirmed by HPLC and 36 mL of a 2M hydrochloric acid solution was dropwise added while taking care to prevent any excess generation of heat. The suspension containing separated solid matter was stirred at 10° C. overnight, the precipitates were isolated through filtration and then dried under reduced pressure at 60° C. to thus obtain 17.32 g of the title compound as a white crystalline solid (yield: 95%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08058432B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-f9bc27c3ea1f4d2a945f7ebc40118fe7
출처 메모uspto-grants-2011_11