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HRID 1789407作成日:2026年10月26日

Hydrochloric Acid → 4-Acetamidonaphthalene-1-sulfonic acid

https://huagongshe.com/reaction/1789407

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物pyridine N-acetyl-1-aminonaphthalene-4-sulphonateHCID 13306497—
溶媒WaterHCID 962—
生成物4-Acetamidonaphthalene-1-sulfonic acidHCID 416995—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04689346
出典データセットuspto-grants-1987_08
ORD IDord-c6d541891e04442aabb122c5d2326b45
出典メモuspto-grants-1987_08