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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28786생성일: 2026년 10월 23일

Sulfuric Acid → Dimethyl (6-methyl-2-oxoheptyl)phosphonate

https://huagongshe.com/ko/reaction/28786

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물5-Methylhexanoic acidHCID 12344—
반응물Dimethyl methylphosphonateHCID 12958—
반응물Methyl 5-methylhexanoateHCID 519894—
반응물ButyllithiumHCID 178418339—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물Dimethyl (6-methyl-2-oxoheptyl)phosphonateHCID 1522396876.2%

반응 단계

To a solution of dimethyl methylphosphonate (2.17 ml, 20 mmol) in anhydrous THF (20 mL), cooled at −78° C. was added n-BuLi (1.6 M in hexane, 13.7 mL, 22 mmol). The mixture was stirred for 30 minutes at this temperature under nitrogen. Methyl 5-methylhexanoate (1.44 g, 10 mmol), prepared from 5-methylhexanoic acid (from Avocado) and methanol at the presence of the catalytic amount of the concentrated sulfuric acid (the procedure described in Intermediate 17.1), was added dropwise for 10 minutes. The mixture was stirred for 2 hours at −78° C., gradually was warm to room temperature. The mixture was quenched with addition of 1N HCl to pH 4-5. The organic layer was separated, washed with brine and dried over MgSO4. The residue was purified through flash chromatography on silica gel (EtOAc:Hexanes=1:1) to give the product (1.80 g) with colorless oil in 76% yield. 1HNMR (CD3OD, ppm) δ 0.866 (d, J=6.5 Hz, 6H), 1.16 (m, 2H), 1.56 (m, 3H), 2.58 (t, J=7.3 Hz, 2H), 3.10 (d, J=22.7 Hz, 2H), 3.70 (s, 3H), 3.79 (s, 3H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419999B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-002ca54a27b442f1985da6a42793eac5
출처 메모uspto-grants-2008_09