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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63616생성일: 2026년 10월 26일

Acetic Acid → 6-Bromo-3,4-dihydronaphthalene-1-carboxamide

https://huagongshe.com/reaction/63616

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sulfuric AcidHCID 1118—
반응물Trimethylsilyl cyanideHCID 82115—
반응물6-Bromo-1-tetraloneHCID 10105069—
촉매zinc(II)iodideHCID 9883512—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물6-Bromo-3,4-dihydronaphthalene-1-carboxamideHCID 11859834380%

반응 조건

온도60 °C

반응 단계

To a solution of 6-bromo-1,2,3,4-tetrahydronaphthalen-1-one (5.46 g, 24.3 mmol) and ZnI2 (50 mg) in toluene (50 mL) was added TMSCN (4.82 mL, 48.6 mmol), and the solution stirred at 60° C. overnight. The reaction was cooled to rt, and H2SO4 (5.6 mL) was added. Then AcOH (34 mL), H2SO4 (25 mL) and H2O (4 mL) were added to the reaction, and it was heated to 105° C. for 3 h. The mixture was cooled and poured over ice-water (250 mL). The precipitate was collected by filtration, washed with water, and dried under vacuum to give 4.88 g (80%) of the title compound as an off-white solid. 1H NMR (400 MHz, DMSO-d6): δ 2.25-2.33 (2H, m), 2.72 (2H, t, J=8.0 Hz), 6.51 (1H, t, J=4.6 Hz), 7.20 (1H, br s), 7.35-7.40 (3H, m), 7.65 (1H, br s). [M+H] calc'd for C11H10BrNO, 252, 254. found 252, 254.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447046B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-6bb6bfdcada2480cbbd54a1d34aaccd8
출처 메모uspto-grants-2016_09