Ethyl pyruvate → HCID 11127054, compound

HRID 1948808Notes

Reaction equation

HRID 1948808 reaction equation
[C:1]1([C@H:7]([CH2:9][OH:10])[NH2:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:11](OCC)(=[O:15])[C:12]([CH3:14])=O>C(O)C(F)(F)F>[CH3:14][C:12]1[C:11](=[O:15])[O:10][CH2:9][C@@H:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[N:8]=1

Participants

4

Reactant 2

HCID 12041Ethyl pyruvateHCID 2724025(R)-beta-aminophenethyl alcohol

Product 1

HCID 11127054HCID 11127054, compoundYield 41%

Reagents, catalysts & solvents 1

HCID 64092,2,2-TrifluoroethanolSolvent

Procedure

(R)-2-phenylglycinol (3.00 g, 21.9 mmol, 1.0 equiv.) and ethyl pyruvate (2.67 mL, 24.1 mmol, 1.1 equiv.) were refluxed in trifluoroethanol (50 mL) over activated 4 molecular sieves (8.00 g) for 24 hours. Filtration through a short pad of CELITE® diatomaceous earth and removal of solvent from the filtrate in vacuo generated the crude product which was purified by flash column chromatography on silica, eluting with petrol and diethyl ether (7:3) to furnish the title compound as a white solid (1.70 g, 41%); mp 71.0-72.0° C. (lit 71.0-72.0° C.); v(max) (KBr) 3001 (C—H), 1734 (C═O), 1642 (C═N) cm−1; δH (250 MHz, CDCl3) 7.42-7.32 (5H, m, Ph), 4.89-4.80 (1H, m, PhCH), 4.56 (1H, dd, /4.49 Hz, T 11.55 Hz, 6β-H), 4.25 (1H, dd, J 10.97 Hz, T 11.51 Hz, 6α-H), 2.40 (3H, s, CH3); δC (62.5 MHz, CDCl3) 160.7, 155.9, 137.2, 129.4, 128.7, 127.5, 71.9, 60.1, 22.2; m/z (CL, NH3), 189 (M+, 25%), 159 (12%), 130 (24%), 104 (100%), 90 (21%), and 78 (6%); HRMS for C11H11NO2 requires 189.0787 found 189.0782. [α]D20 −2560.0 (c 1.11 CHCl3) (lit [α]D20 −237.1 (c 1.11 CHCl3)).

Workup

  1. customfor 24 hours
  2. filtrationFiltration
  3. customthrough a short pad of CELITE® diatomaceous earth and removal of solvent from the filtrate in vacuo
  4. customwas purified by flash column chromatography on silica
  5. washeluting with petrol and diethyl ether (7:3)

Sources & evidence

ORD record
ord-94a1d70e8d18459da21663db77eba318
Source dataset
uspto-grants-2013_03
Patent number
US08399612B2

Reaction notes

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