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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1591040생성일: 2026년 10월 26일

2-Chloronaphthalene → 2-(2-Naphthyl)-6-hydroxybenzoxazole

https://huagongshe.com/reaction/1591040

반응식

참여 물질

역할이름HCID투입량
반응물2-ChloronaphthaleneHCID 7056—
반응물TetrahydrofuranHCID 8028—
반응물Sodium HydroxideHCID 14798—
반응물4-Aminobenzene-1,3-diol hydrochlorideHCID 13408822—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물2-(2-Naphthyl)-6-hydroxybenzoxazoleHCID 1976602747.5%

반응 단계

20 g (104.9 mmol) of 2-naphthyl chloride and 2.5 g (15.5 mmol) of 4-aminoresorcinol hydrochloride were introduced into a three-necked flask provided with a thermometer and a cooling condenser, and the mixture was heated at 135° to 205° C. for 1 hour, then excessive acid chloride was removed by distillation. To the residue, 8.3 g (207.5 mmol) of NaOH, 60 ml of THF, 60 ml of water and 30 ml of methanol were added, and the mixture was stirred at room temperature for about 2 hours. The reaction solution was extracted with ethyl acetate, the extract was washed with saturated sodium chloride water solution, and ethyl acetate was distilled off. Recrystallizing the residue with water/methanol/THF and drying the crystal, there was obtained 1.92 mg (7.36 mmol) of 2-(2-naphthyl)-6-hydroxybenzoxazole. The yield was 47.5%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05206149
출처 데이터셋uspto-grants-1993_04
ORD IDord-7d59f3617b824bcdb9d430a7dd9c0ccb
출처 메모uspto-grants-1993_04