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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 629139생성일: 2026년 10월 27일

Hydrochloric Acid → 5-(3,3-Dimethylbutyl)thiophene-2-carbaldehyde

https://huagongshe.com/reaction/629139

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DimethylformamideHCID 6228—
반응물ThiopheneHCID 8030—
반응물1-Chloro-3,3-dimethylbutaneHCID 76111—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexamethylphosphoramideHCID 12679—
생성물5-(3,3-Dimethylbutyl)thiophene-2-carbaldehydeHCID 11822896619%

반응 조건

온도-78 °C

반응 단계

To a solution of thiophene (300 mg, 3.57 mmol) in anhydrous 10% hexamethylphosphoramide in tetrahydrofuran (33 mL) under argon at −78° C. was added n-butyllithium (1.57 mL, 2.5 M in hexanes) dropwise. After stirring at −78° C. for 1 hour, 1-chloro-3,3-dimethylbutane (430 mg, 3.57 mmol) was added dropwise and the resulting solution allowed to warm to room temperature over 3 hours. The reaction mixture was re-cooled to −78° C., a second portion of n-butyllithium (1.78 mL, 4.46 mmol) was added dropwise over 5 minutes and the mixture was stirred for 1 hour at −78° C. before anhydrous dimethylformamide (1.38 mL, 17.8 mmol) was added dropwise and the resulting mixture allowed to warm to room temperature. The reaction mixture was poured into 1 N hydrochloric acid (150 mL) and organics were extracted with ether (3×100 mL), dried with magnesium sulfate, filtered and concentrated. The residue was purified by flash chromatography on silica gel with gradient elution (5%→20% ethyl acetate in hexanes) to give 5-(3,3-dimethylbutyl)thiophene-2-carbaldehyde (130 mg, 19%). Used without further characterization.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09315495B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-217d810fc451467987b2a2654e9fb484
출처 메모uspto-grants-2016_04