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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 356522생성일: 2026년 10월 24일

Methyl acetoacetate → 4-Hydroxy-6,6-diphenethyl-5,6-dihydro-pyran-2-one

https://huagongshe.com/ko/reaction/356522

반응식

참여 물질

역할이름HCID투입량
반응물Methyl acetoacetateHCID 7757—
반응물1,5-Diphenylpentan-3-oneHCID 21496—
반응물Sodium hydrideHCID 24758—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물4-Hydroxy-6,6-diphenethyl-5,6-dihydro-pyran-2-oneHCID 54711545—

반응 단계

Freshly distilled THF (25 mL) was cooled in an ice bath under a nitrogen atmosphere, then charged with 660 mg (16.5 mmol) sodium hydride (60% dispersion). This suspension was treated with 1.89 g (16.3 mmol) methyl acetoacetate dropwise, and the reaction was stirred for 10 minutes. n-Butyllithium (10.3 mL of 1.6M in hexanes; 16.5 mmol) was dripped in and the reaction was stirred 30 minutes. At this time 3.10 g (13 mmol) of 1,5-diphenyl-3-pentanone (Ram and Spicer, Tetrahedrom Lett., 1988, 29 (31), 3741) in 20 mL THF was added dropwise over 15 minutes. After 4 hours 100 mL H2O was added and the reaction stirred overnight. The reaction was extracted with diethyl ether, and the organics set aside. The aqueous layer was chilled, treated with 50% HOAc until a precipitate formed, and then extracted with EtOAc. These organics were washed with saturated brine, dried (Na2SO4), and concentrated. 1H NMR (DMSO-d6) δ 2.0 (d of d, 4 H), 2.65 (m, 6 H), 5.0 (s, 1 H), 7.15-7.35 (m, 10 H), 11.4 (bs, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05834506
출처 데이터셋uspto-grants-1998_11
ORD IDord-39ad07d5e0ba49a1a03f0075c416c642
출처 메모uspto-grants-1998_11