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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 480449생성일: 2026년 10월 24일

2-Hydroxy-1-naphthaldehyde → 6-Bromo-2-hydroxy-1-naphthaldehyde

https://huagongshe.com/ko/reaction/480449

반응식

참여 물질

역할이름HCID투입량
반응물2-Hydroxy-1-naphthaldehydeHCID 12819—
반응물BromineHCID 24408—
반응물Sodium ThiosulfateHCID 24477—
용매Acetic AcidHCID 176—
생성물6-Bromo-2-hydroxy-1-naphthaldehydeHCID 73545732.9%

반응 단계

To a solution of 2-hydroxy-1-naphthaldehyde (60.0 g) in AcOH (300 mL) was added dropwise a solution of bromine (66.8 g) in AcOH (30 mL) over 30 min. After being stirred for 1 h, the mixture was poured into aqueous Na2S2O3 solution, and the resulting mixture was extracted with AcOEt. The combined organic layers were washed with water, 1N-NaOH, and brine followed by drying over MgSO4. After removal of the solvent in vacuo, the residue was washed with EtOH to give a yellow powder. The powder was crystallized from iPrOH to afford the title compound (28.8 g) as pale yellow needles.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06649643B1
출처 데이터셋uspto-grants-2003_11
ORD IDord-a87524f6e97d4e8f8078701930375b8b
출처 메모uspto-grants-2003_11