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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1789407생성일: 2026년 10월 26일

Hydrochloric Acid → 4-Acetamidonaphthalene-1-sulfonic acid

https://huagongshe.com/reaction/1789407

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물pyridine N-acetyl-1-aminonaphthalene-4-sulphonateHCID 13306497—
용매WaterHCID 962—
생성물4-Acetamidonaphthalene-1-sulfonic acidHCID 416995—

반응 단계

15 g (0.04 mole) of pyridine N-acetyl-1-aminonaphthalene-4-sulphonate is dissolved in the minimum amount of water in an Erlenmeyer flask. This solution is conveniently cooled and is acidified with concentrated hydrochloric acid, following which the precipitate formed is collected in a filter to give N-acetyl-1-amino-4-naphthalenesulphonic acid, which is then filtered, washed and dried, and suspended in water. An aqueous solution of the stoichiometric amount of tranexamic acid (AMCHA) is then added, and the mixture is stirred for 15 minutes at ambient temperature and evaporated to dryness. The residue obtained is recrystallized in absolute alcohol, 14.1 g (Yield 76.6%) of AMCHA N-acetyl-1-aminonaphthalene-4-sulphonate finally being obtained, whose m.p. is 214°-215° C. and whose IR spectrum (KBr) has the following bands: 1,670; 1,650; 1,530; 1,510; 1,370; 1,320; 1,200; 1,040; 750; 670; 640.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04689346
출처 데이터셋uspto-grants-1987_08
ORD IDord-c6d541891e04442aabb122c5d2326b45
출처 메모uspto-grants-1987_08