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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1591114생성일: 2026년 10월 25일

Triethylamine → 1-(4-Carbomethoxyphenyl)-4-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-butane-1,4-dione

https://huagongshe.com/reaction/1591114

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methyl 4-FormylbenzoateHCID 15294—
반응물6-(3-Chloropropionyl)-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthaleneHCID 14726511—
촉매3-Benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chlorideHCID 2833352—
용매DimethylformamideHCID 6228—
생성물1-(4-Carbomethoxyphenyl)-4-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-butane-1,4-dioneHCID 1472649245.5%

반응 단계

5.6 g (0.02 mole) of 6-(3-chloropropionyl)-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnapthalene and 3.3 ml (0.024 mole) of triethylamine in 30 ml of dimethylformamide were stirred for 1 hour at room temperature. Thereafter, a solution of 3.6 g (0.025 mole) of methyl 4-formylbenzoate and 1 g of 3-benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chloride in 10 ml of dimethylformamide was added dropwise. Stirring was continued for 1 hour, after which the mixture was poured onto ice/water and extracted twice with ethyl acetate, and the combined organic extracts were washed several times with water, dried over magnesium sulfate and evaporated down. 3.7 g of 1-(4-carbomethoxyphenyl)-4-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-butane-1,4-dione of melting point 139°-141° C. were obtained from the residue (6.4 g) after recrystallization from ethanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05206242
출처 데이터셋uspto-grants-1993_04
ORD IDord-2d768b8697394d8b83e07f06b10a38a1
출처 메모uspto-grants-1993_04