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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 984705생성일: 2026년 10월 27일

Ammonia → 7-Bromonaphthalen-2-amine

https://huagongshe.com/reaction/984705

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Hydrochloric AcidHCID 313—
반응물7-Bromo-2-naphtholHCID 613827—
반응물Diammonium sulfite monohydrateHCID 21701053—
용매Ethyl AcetateHCID 8857—
생성물7-Bromonaphthalen-2-amineHCID 22240243—

반응 조건

온도150 °C

반응 단계

According to the procedure described in the aforementioned reference [L. C. Anderson et al., Journal of the American Chemical Society (J. Am. Chem. Soc.), vol. 65, p.241, 1943], 2-bromo-7-hydroxynaphthalene (2.23 g, MAYB) was added with 30% aqueous ammonia (30 ml) and ammonium sulfite monohydrate (2.69 g, WAKO) and stirred in a shield tube at 150° C. for 27 hours. The reaction mixture was added with ethyl acetate (90 ml) for extraction and then added with 1 N aqueous hydrochloric acid (1.5 l). The aqueous layer was separated, washed with ethyl acetate, then neutralized by adding 5 N aqueous sodium hydroxide (300 ml) under ice cooling and extracted with ethyl acetate again. The organic layer was washed with saturated brine and dried, and then the solvent was evaporated under reduced pressure to obtain the title compound (Intermediate 26, 1.00 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06867320B2
출처 데이터셋uspto-grants-2005_03
ORD IDord-9004eef9bbb94dbe824324702ec59b15
출처 메모uspto-grants-2005_03