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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2260934생성일: 2026년 10월 26일

1-(2,6,6-Trimethylcyclohex-3-en-1-yl)but-2-en-1-one → Methyl 2-(4-oxo-4-(2,6,6-trimethylcyclohex-3-enyl)butan-2-ylamino)-3-(4-oxo-4-(2,6,6-trimethylcyclohex-3-enyl)butan-2-ylthio)propanoate

https://huagongshe.com/reaction/2260934

반응식

참여 물질

역할이름HCID투입량
반응물1-(2,6,6-Trimethylcyclohex-3-en-1-yl)but-2-en-1-oneHCID 42296—
반응물DiisopropylethylamineHCID 81531—
반응물L-Cysteine, methyl ester, hydrochlorideHCID 2733208—
용매MethanolHCID 887—
생성물Methyl 2-(4-oxo-4-(2,6,6-trimethylcyclohex-3-enyl)butan-2-ylamino)-3-(4-oxo-4-(2,6,6-trimethylcyclohex-3-enyl)butan-2-ylthio)propanoateHCID 6863587882%

반응 단계

A solution of 1-(2,6,6-trimethylcyclohex-3-enyl)but-2-en-1-one (19.28 g, 100 mmol, 2 equiv.), ethyl diisopropylamine (6.45 g, 50 mmol, 1 equiv.) and L-Cystein methyl ester hydrochloride (8.60 g, 50 mmol, 1 equiv.) in MeOH (120 ml) is heated to reflux during 28 h. The solvent is removed in vacuo and the residue dissolved in methyl t-butyl ether. The solution is washed with dilute aq. NaCl, dried over MgSO4 and concentrated. The residue is purified by chromatography on SiO2 to yield 21.3 g (82%) of the title compound as yellowish, viscous oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07846887B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-c9b7ced433ec4f2986752cd133d4161c
출처 메모uspto-grants-2010_12