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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 707466생성일: 2026년 10월 26일

Dichloromethane → HCID 178519325, 화합물

https://huagongshe.com/reaction/707466

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참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물1,2-DimethoxyethaneHCID 8071—
반응물1H-Pyrazole-5-boronic acidHCID 11251979—
반응물4-Bromo-5-nitrothiophene-2-carbaldehydeHCID 21886281—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
용매WaterHCID 962—
용매TriethylamineHCID 8471—
생성물HCID 178519325HCID 178519325100.4%

반응 조건

온도80 °C

반응 단계

A flask containing 4-bromo-5-nitrothiophene-2-carbaldehyde (1.00 g, 4.24 mmol), (1H-pyrazol-5-yl)boronic acid (510 mg, 4.56 mmol), ethyleneglycol dimethyl ether (20 mL), triethylamine (1.80 mL), water (2.00 mL) and bis(diphenylphosphino)ferrocene]dichloropalladium(II) complex with dichloromethane (340 mg, 0.42 mmol) was evacuated and purged with nitrogen twice, then heated at 80° C. under nitrogen for 4 h. The reaction was cooled to room temperature, poured into a saturated solution of ammonium chloride (20 mL), extracted with ethyl acetate (3×10 mL), combined organics washed with a saturated solution of ammonium chloride (30 mL), dried (Na2SO4) and concentrated under reduced pressure. The crude product was purified by flash chromatography, eluting with ethyl acetate in hexanes, to yield 5-nitro-4-(1H-pyrazol-3-yl)thiophene-2-carbaldehyde as a yellow oil (950 mg, 28%). 1H NMR (400 MHZ, DMSO-d6) δ 6.99 (s, 1H), 7.94 (s, 1H), 8.42 (s, 1H), 10.07 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09175010B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-ceebab437e3f454a9bd99cf7b5456914
출처 메모uspto-grants-2015_11