Potassium Carbonate → HCID 86704610, compound

HRID 1508555Notes

Reaction equation

HRID 1508555 reaction equation
[OH:1][C:2]1[C:3]([I:12])=[C:4]([CH:7]=[CH:8][C:9]=1[O:10][CH3:11])[CH:5]=O.C(=O)([O-])[O-].[K+].[K+].C(OP([CH2:27][C:28]([O:30][CH3:31])=[O:29])(OCC)=O)C>CO>[OH:1][C:2]1[C:3]([I:12])=[C:4](/[CH:5]=[CH:27]/[C:28]([O:30][CH3:31])=[O:29])[CH:7]=[CH:8][C:9]=1[O:10][CH3:11]

Participants

5

Conditions

Temperature
55 °C

Procedure

To a solution of 3-hydroxy-2-iodo-4-methoxybenzaldehyde (2.5 g, 8.99 mmol) in methanol (30 ml) was added potassium carbonate (3.11 g, 22.48 mmol) and methyl diethylphosphonoacetate (1.980 ml, 10.79 mmol). The initial cloudy mixture became clear with the addition of the base (although the base itself was mostly insoluble) The mixture was stirred overnight at 55° C. and became yellow and cloudy again. The solution was then concentrated in vacuo and the residue was taken up in ethyl acetate (20 mL) and 1M HCl (aq) (20 mL). The organic layer was separated and washed with brine (1×20 mL), dried over sodium sulfate, concentrated in vacuo, and purified via column chromatography on a Biotage 65i column eluting with 0% ethyl acetate in hexanes (1 CV) followed by a gradient to 50% ethyl acetate in hexanes (over 7 CV) to furnish the desired product as the E olefin. 1H NMR (CDCl3, 500 MHz) $ 7.95 (d, J=15.9 Hz, 1H), 7.14 (d, J=8.4 Hz, 1H), 6.74 (d, J=8.6 Hz, 1H), 6.27 (d, J=15.8 Hz, 1H), 3.91 (s, 3H), 3.80 (s, 3H), 2.34 (s, 3H).

Workup

  1. additionThe initial cloudy mixture became clear with the addition of the base (although the base itself
  2. concentrationThe solution was then concentrated in vacuo
  3. customThe organic layer was separated
  4. washwashed with brine (1×20 mL)
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated in vacuo
  7. custompurified via column chromatography on a Biotage 65i column
  8. washeluting with 0% ethyl acetate in hexanes (1 CV)

Sources & evidence

ORD record
ord-16899ceaaec443d6a7ee504c77f5ddbb
Source dataset
uspto-grants-2015_12
Patent number
US09221834B2

Reaction notes

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