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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 555429생성일: 2026년 10월 26일

2-Tert-Butylphenol → 2-(2-Tert-butylphenoxy)-3-nitrothiophene

https://huagongshe.com/reaction/555429

반응식

참여 물질

역할이름HCID투입량
반응물2-Tert-ButylphenolHCID 6923—
반응물Potassium CarbonateHCID 11430—
반응물2-Chloro-3-nitrothiopheneHCID 220186—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물2-(2-Tert-butylphenoxy)-3-nitrothiopheneHCID 59857371—

반응 조건

온도105 °C

반응 단계

To a solution of 2-chloro-3-nitrothiophene (1.13 g, 6.93 mmol) in NMP (10 mL) in a pressure vessel was added 2-tert-butylphenol (1.04 g, 6.93 mmol) and K2CO3 (1.0 g, 10.1 mmol). The reaction was flushed with nitrogen, sealed and then heated to 105° C. for 48 h. The reaction was cooled to rt, diluted with EtOAc (˜150 mL) and washed twice with saturated aqueous NaCl (2ט150 mL). The aqueous washes were then back extracted with EtOAc. The combined organics were dried over MgSO4, filtered and concentrated to yield the crude desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08053450B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-eb9dfcffa5234e0e81072bfdd967b62b
출처 메모uspto-grants-2011_11