돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 359660생성일: 2026년 10월 26일

Hydrochloric Acid → N-(4-Carboxybenzyl)-(2-naphthoxy)acetamide

https://huagongshe.com/reaction/359660

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물ChlorotrimethylsilaneHCID 6397—
반응물2-Naphthoxyacetic acidHCID 8422—
반응물4-(Aminomethyl)Benzoic AcidHCID 65526—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물N-(4-Carboxybenzyl)-(2-naphthoxy)acetamideHCID 13922246—

반응 단계

(2-Naphthoxy)acetic acid (8.5 g) is suspended in 160 mL methylene chloride and treated with 1,1'-carbonyldiimidazole (6.8 g) which is added in small portions. After stirring for 3 hrs at room temperature under a nitrogen atmosphere, the mixture is added dropwise to a previously prepared solution of alpha-amino-p-toluic acid (1.4 g), chlorotrimethylsilane (10 mL), and triethylamine (11 mL) in 250 mL methylene chloride at 0° C. The final mixture is stirred at room temperature under a nitrogen atmosphere overnight. The mixture is combined with 200 mL 1 N HCl and shaken, after which the resultant precipitate is collected by suction filtration. The precipitate is recrystallized from methanol/2N HCl, m.p. 188°-189° C. as N-(4-carboxybenzyl)-(2-naphthoxy)acetamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05002703
출처 데이터셋uspto-grants-1991_03
ORD IDord-0aa585abb3e4471a82cf99f8e131bd05
출처 메모uspto-grants-1991_03