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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 612571생성일: 2026년 10월 25일

2-Amino-2-phenylethan-1-ol → (S)-(+)-3,4-dihydroxy-5-methyl-5-[4-(2-methylpropyl)phenyl]-2(5H)-furanone

https://huagongshe.com/reaction/612571

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-2-phenylethan-1-olHCID 134797—
반응물Methyl (alphaS)-alpha-methyl-4-(2-methylpropyl)benzeneacetateHCID 6933487—
반응물Ethyl 4-iso-butylbenzoylformateHCID 12585534—
생성물(S)-(+)-3,4-dihydroxy-5-methyl-5-[4-(2-methylpropyl)phenyl]-2(5H)-furanoneHCID 7024796019%

반응 단계

(S)-(+)-3,4-Dihydroxy-5-methyl-5-[4-(2-methylpropyl)phenyl]-2(5H)-furanone was synthesized in an analogous manner used for the production of(R)-(-)-5-[(1,1'-biphenyl)-4-yl]-3,4-dihydroxy-5-methyl-2(5H)-furanone starting with ethyl 4-isobutylbenzoylformate. (S)-(+)-Phenylglycinol was used to resolve the methyl (S)-(+)-2-(4-isobutylphenyl)propionate enantiomer, of which 1.2 g (5 mmol) was converted into 250 mg (19% yield) of (S)-(+)-3,4-dihydroxy-5-methyl-5-[4-(2-methylpropyl)phenyl]-2(5H)-furanone as a white crystalline material: mp 175-177° C. dec. (CHCl3 /hexanes); [α]25D +132° (c=1.55; MeOH) 1H NMR (acetone-d6) δ 7.44-7.14 (m, 4H), 2.48 (d, 2H, J=7.1 Hz), 1.87-1.82 (m, 1H), 1.83 (s, 3H), 0.88 (d, 6H, J=6.5 Hz). Anal Calcd for C15H18O4 : C, 68.68; H, 6.92. Found: C, 68.08; H, 6.90.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06005000
출처 데이터셋uspto-grants-1999_12
ORD IDord-9ded5f90fb4d4cc58fc081043067ec02
출처 메모uspto-grants-1999_12