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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 347315생성일: 2026년 10월 25일

Tetrahydrofuran → 5,5,8,8-Tetramethyl-5,6,7,8-tetrahydro-2-naphthalenecarbaldehyde

https://huagongshe.com/reaction/347315

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물6-Bromo-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthaleneHCID 226685—
반응물ButyllithiumHCID 178418339—
생성물5,5,8,8-Tetramethyl-5,6,7,8-tetrahydro-2-naphthalenecarbaldehydeHCID 10420887100%

반응 조건

온도-70 °C

반응 단계

A flame dried round bottom flask was charged with 6-bromo-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphtalene (10 g, 37 mmol) and anhydrous THF (100 mL). This solution was cooled to −70° C. while stirring under a nitrogen blanket. To this solution was added 2.5 M n-butyl lithium (14.9 mL, 37 mmol). The reaction mixture was allowed to stir for 30 minutes at which time it was quenched via the addition of dimethylformamide (5.0 mL). The reaction was allowed to warm to RT where it stirred for 17 hours. The reaction was quenched by the addition of 1.0 N HCl (100 mL). The reaction mixture was extracted using ether. The organics were separated and dried over MgSO4 followed by concentrating to dryness. The resulting oil was dried under high vacuum to give a total of 8.2 g (100%) of crude oil. The product was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07173134B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-4bf8a7d3b75445f48227557759f7aa47
출처 메모uspto-grants-2007_02