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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1375264생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1375264

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물DimethylformamideHCID 6228—
반응물PentaneHCID 8003—
반응물TetrahydrofuranHCID 8028—
반응물1-(5-Methyl-thien-2-yl)3,4-dihydro-4,4-dimethyl-7-bromo-naphthaleneHCID 18620062—
반응물HCID 178418306HCID 178418306—
용매Diethyl EtherHCID 3283—
생성물1(5-Methyl-thien-2-yl)3,4-dihydro-4,4-diethyl-7-naphthaldehydeHCID 21079515—

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 번호US07166726B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-0dfef76ef84349f897b21b46838ad55b
출처 메모uspto-grants-2007_01