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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75154생성일: 2026년 10월 23일

Tricyclo(3.3.1.13,7)dec-1-ylmethylamine → N-(1-adamantylmethyl)-5-methyl-3-oxohexanamide

https://huagongshe.com/ko/reaction/75154

반응식

참여 물질

역할이름HCID투입량
반응물Tricyclo(3.3.1.13,7)dec-1-ylmethylamineHCID 86625—
반응물2,2-Dimethyl-5-(3-methylbutanoyl)-1,3-dioxane-4,6-dioneHCID 59437173—
용매1,4-DioxaneHCID 31275—
생성물N-(1-adamantylmethyl)-5-methyl-3-oxohexanamideHCID 5943716254.4%

반응 단계

A solution of 5-(3-methylbutanoyl)-2,2-dimethyl-1,3-dioxane-4,6-dione (2.76 g, 12 mmol) and (1-adamantylmethyl)amine (2 g, 12 mmol) in anhydrous 1,4-dioxane (10 mL) was heated under reflux for 2 h. Solvent was removed in vacuo. The residue was diluted with EtOAc (50 mL), washed with water, aq K2CO3 and brine, dried over Na2SO4 and concentrated to dryness. The residue was purified by chromatography on a silica gel column eluted with 20:1 PE/EtOAc to give the N-(1-adamantylmethyl)-5-methyl-3-oxohexanamide (1.90 g, 54.4%). 1H NMR: (400 MHz, CDCl3): δ=0.92 (s, 3H), 0.96 (s, 3H), 1.54 (s, 7H), 1.62-1.73 (m, 9H), 1.98 (s, 4H), 2.12(m, 1H), 2.45(d, 2H), 2.95(d, 2H), 3.65(s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835426B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-0ecc176c213940abade3d063b7446509
출처 메모uspto-grants-2014_09