Tetrahydrofuran → (1R*,2R*)-Acetic acid 1-hydroxy-1,2-dihydro-naphthalen-2-yl-ester

HRID 1060706

반응식

HRID 1060706 반응식
[C:1]([O-:4])(=[O:3])[CH3:2].[Na+].Cl.C(N([CH2:12][CH3:13])CC)C.[CH2:14]1[CH2:18][O:17][CH2:16][CH2:15]1>C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.[Fe+2]>[OH:17][C@@H:16]1[C:12]2[C:13](=[CH:18][CH:14]=[CH:15][CH:16]=2)[CH:18]=[CH:14][C@H:15]1[O:3][C:1](=[O:4])[CH3:2]

참가 물질

5

반응물 3

HCID 8028TetrahydrofuranHCID 11130Triethylamine hydrochlorideHCID 517045Sodium Acetate

생성물 1

HCID 9837127(1R*,2R*)-Acetic acid 1-hydroxy-1,2-dihydro-naphthalen-2-yl-ester

시약·촉매·용매 1

HCID 635956Ferrocene-1,1'-bis-(diphenylphosphine)촉매

실험 절차

To a flame dried round bottom flask, [Rh(COD)Cl]2 (4.3 mg, 0.008 mmol DPPF (9.6 mg, 0.017 mmol), 1 (50 mg, 1.39 mmol), and sodium acetate (142 mg, 1.74 mmol) were added followed by addition of THF (2 mL) and triethylamine hydrochloride (239 mg, 1.74 mmol). The mixture was heated at reflux for 3 hours and the solvents were removed in vacuo. The resulting mixture was purified by flash chromatography (30% ethyl acetate in hexanes) to give 2 as a crystalline solid (41 mg), 63%). Rf=0.26 on silica gel (20% ethyl acetate:hexanes); mp 67-68° (Et2O); IR (KBr, cm−1) 1H NMR (400 MHz, CDCl3) δ7.54-7.53 (1H, m), 7.29-7.24 (2H, m), 7.10-7.08 (1H, m), 6.50 (1H, dd,J=3.9, 1.3 Hz), 5.85 (1H, dd, J=9.9, 3.1 Hz), 5.59 (1H, ddd, J=9.0, 2.8, 1.9 Hz), 4.92 (1H, d, J=9.0 Hz), 2.64 (1H, s), 2.12 (3H, s); 13C NMR (400 MHz, CDCl3) δ171.3, 135.2, 131.5, 129.5, 128.3, 126.7, 126.0, 125.4, 75.3, 71.7, 21.2. HRMS calcd for C12H12O3 (M−): 204.0786. Found: 204.0791.

후처리

  1. customTo a flame dried round bottom flask
  2. temperatureThe mixture was heated
  3. temperatureat reflux for 3 hours
  4. customthe solvents were removed in vacuo
  5. customThe resulting mixture was purified by flash chromatography (30% ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-60373af8af2b4590bc23b830e39b27f7
출처 데이터셋
uspto-grants-2003_02
특허 번호
US06525068B1

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