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HRID 2392813생성일: 2026년 10월 24일

Hydrochloric Acid → 2-Nitroso-1-naphthol

https://huagongshe.com/ko/reaction/2392813

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1-Nitroso-2-naphtholHCID 8580—
반응물Sodium HydroxideHCID 14798—
반응물Sodium DithioniteHCID 24489—
반응물1-Amino-2-naphthol hydrochlorideHCID 518469—
용매WaterHCID 962—
생성물2-Nitroso-1-naphtholHCID 8592—

반응 조건

온도20 °C

반응 단계

48 g of 1-nitroso-2-naphthol are suspended in a mixture of 300 ml of water and 60 ml of 5n NaOH, then another 240 ml of 5n NaOh are added. While stirring well hot water vapor is passed through the solution until the temperature reaches 35° C. Subsequently 120 g of freshly prepared sodium dithionite is added with the temperature rapidly rising to 60° C. The solution assumes an amber-colored tint. After 15 minutes, the solution is rapidly cooled to under 20° C. by adding 200 g of ice and 100 ml of concentrated hydrochloric acid. The white, flaky precipitation is filtered by vacuum and suspended in a mixture of 500 ml of water and 50 ml concentrated hydrochloric acid. Overheated water vapor is passed into this mixture with such a volume flow that the temperature reaches 90° C. within 10 min. At this temperature is stirred another hour while reducing the vapor flow. The still hot solution is filtered with the aubergine-colored precipitation remaining. Upon cooling the filtrate, a light, flaky precipitation falls out which is sucked away, scavenged with diluted hydrochloric acid and then with ether and dried. Yielded were 45 g of 1-amino-2-naphthol-hydrochloride. The amino-hydroxy aromatic compounds were employed in all the transformations into this acidic form, because the free bases with the exception of 5-amino-6-quinoline proved to be very unstable.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05801243
출처 데이터셋uspto-grants-1998_09
ORD IDord-186c76bf8c6b4f44980252642b2ccb85
출처 메모uspto-grants-1998_09