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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2609생성일: 2026년 10월 23일

Carbon Dioxide → 1(5-Methyl-thien-2-yl) 3,4-dihydro-4,4-dimethyl-7-naphthaldehyde

https://huagongshe.com/ko/reaction/2609

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물DimethylformamideHCID 6228—
반응물PentaneHCID 8003—
반응물1-(5-Methyl-thien-2-yl)3,4-dihydro-4,4-dimethyl-7-bromo-naphthaleneHCID 18620062—
반응물HCID 178418306HCID 178418306—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물1(5-Methyl-thien-2-yl) 3,4-dihydro-4,4-dimethyl-7-naphthaldehydeHCID 18620066—

반응 단계

To a cold (-78° C.) solution of 1-(5-methyl-thien-2-yl)-3,4-dihydro-4,4-dimethyl-7-bromo-naphthalene (Compound F, 1.35 g, 4.1 mmol), in THF (20 mL) was added t-BuLi in pentane (1.7M solution, 3.5 mL, 5.95 mmol). The reaction was stirred for 15 minutes and DMF (600 mg, 5.8 mmol) was added and dry-ice cooling was replaced with ice-water bath. The mixture was stirred at ambient temperature for 4 hours. The reaction mixture was diluted with ether (70 mL) and washed with water (5 mL), brine (5 mL) and dried with MgSO4. Solvent was removed by distillation. The product was purified by silicagel chromatography to afford the title compound as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728846
출처 데이터셋uspto-grants-1998_03
ORD IDord-4955e9d4488f4c70a01e631513107eb7
출처 메모uspto-grants-1998_03