돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1732생성일: 2026년 10월 23일

Water → N-(3,4-dihydro-2H-naphthalen-1-ylidene)hydroxylamine

https://huagongshe.com/ko/reaction/1732

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-TetraloneHCID 10724—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물Sodium AcetateHCID 517045—
용매EthanolHCID 702—
생성물N-(3,4-dihydro-2H-naphthalen-1-ylidene)hydroxylamineHCID 7687695%

반응 조건

온도75 °C

반응 단계

To 4.6 L of water at room temperature in a 4-neck 50 L flask sitting in a steam bath apparatus equipped with an overhead stirrer, a temperature probe and reflux condenser was added 3.72 Kg (27.36 mol) of sodium acetate with stirring, followed by 1.9 Kg of hydroxylamine hydrochloride (27.36 mol). To this slurry at room temperature, 12 L of ethanol was added followed by 1.994 Kg (13.68 mol) of 1-tetralone. Additional ethanol (1.7 L) was used to rinse off the funnel and added to the reaction mixture. The resulting light orange slurry was heated to 75° C. over 40 minutes and maintained at 75°-85° C. for another 75 minutes. The reaction mixture was cooled with the aid of ice packed around the flask. When the internal temperature reached 32° C., the reaction mixture was pumped over 15 minutes into 60 L of ice contained in a 200 L vessel. The reaction vessel was washed with an additional 2 L of water which was added to the 200 L vessel. When the ice melted, the mixture was filtered through a filter pad and the wet cake washed with 4 L of water. The wet cake was suction dried for 1 hour then transferred to two trays and dried under vacuum at 40° C. for 2 days to give 2.094 Kg (13.01 mol, 95%) of product. 1H NMR (250 MHz,CDCl3): 1.90 (m,2H), 2.80 (t,6 Hz,2H), 2.88 (t,6 Hz,2H), 7.15-7.35 (m,3H), 7.90 (d,8 Hz,1H), 8.9 (br s,1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726307
출처 데이터셋uspto-grants-1998_03
ORD IDord-377a459ff6984e289cfcd5758d18e946
출처 메모uspto-grants-1998_03