Ethyl pyruvate → HCID 11127054, compound

HRID 1666918Notes

Reaction equation

HRID 1666918 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

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-22e57005af214d75b0c2fdd312a78150
Source dataset
uspto-grants-2011_10
Patent number
US08044173B2

Reaction notes

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