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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1107144생성일: 2026년 10월 25일

Isopropylamine → Methyl 3-hydroxy-3-isopropyl-7-phenylheptanoate

https://huagongshe.com/reaction/1107144

반응식

참여 물질

역할이름HCID투입량
반응물IsopropylamineHCID 6363—
반응물Methyl isovalerateHCID 11160—
반응물BenzenepentanalHCID 561886—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물Methyl 3-hydroxy-3-isopropyl-7-phenylheptanoateHCID 18790185—

반응 조건

온도-78 °C

반응 단계

To a solution of 2.4 mL (18.49 mmol, 1.5 eq) of isopropylamine in 50 mL of dry THF at -78° C. under argon is added 9.3 mL (14.8 mmol, 1.2 eq) of 1.6 M BuLi in hexanes solution. This is stirred at -78° C. for 1 hour at which time 1.8 mL (13.56 mmol, 1.1 eq) of methyl isovalerate is added dropwise. This mixture is stirred at -78° C. for 1.5 hours at which time 2 g (12.33 mmol) of 5-phenylpentanal in 10 mL of dry THF is added dropwise. This is stirred at -78° C. for 1 hour, then allowed to warm slowly to 0° C. over 3 hours. The reaction is quenched with saturated NH4Cl solution and then partitioned between ether and saturated NH4Cl solution. The organics are dried (Na2SO4) and concentrated in vacuo. The product is purified by flash silica gel chromatography to afford methyl 3-hydroxy-3-isopropyl-7-phenylheptanoate in the form of a yellow oil. (0.88 g, 26%): 1H-NMR (300 MHz, CDCl3) δ (TMS) 0.95(t, 6H), 1.45(m, 3H), 1.6(m, 3H), 2.08(bs, 1H), 2.15(m, 1H), 2.35(t, 1H), 2.6(t, 2H), 3.68(s, 3H), 3.85(bm, 1H), 7.15(m, 3H), 7.25(m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06057369
출처 데이터셋uspto-grants-2000_05
ORD IDord-0ef565c4a07a4253b81827196914cfc3
출처 메모uspto-grants-2000_05