Carbon Dioxide → HCID 59233701, compound

HRID 219344Notes

Reaction equation

HRID 219344 reaction equation
C(=O)=O.[F:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[S:15][C:14]3[CH:16]=[CH:17][C:18]([O:20][CH3:21])=[CH:19][C:13]=3[C:12]=2I)=[CH:7][CH:6]=1.C([Li])CCC.[CH3:28][O:29][C:30](Cl)=[O:31]>C1COCC1.CC(C)=O>[F:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[S:15][C:14]3[CH:16]=[CH:17][C:18]([O:20][CH3:21])=[CH:19][C:13]=3[C:12]=2[C:30]([O:29][CH3:28])=[O:31])=[CH:7][CH:6]=1

Participants

7

Reactant 4

HCID 280Carbon DioxideHCID 6586Methyl chloroformateHCID 592336892-(4-Fluorophenyl)-3-iodo-5-methoxybenzo[b]thiopheneHCID 178418339Butyllithium

Product 1

HCID 59233701HCID 59233701, compound

Reagents, catalysts & solvents 2

HCID 180AcetoneSolventHCID 8028TetrahydrofuranSolvent

Conditions

Temperature
-78 °C

Procedure

To a cooled solution (−78° C., dry ice, acetone) containing 2-(4-fluorophenyl)-3-iodo-5-methoxybenzo[b]thiophene (1.0 g, 2.6 mmol,) and THF (26 mL) was added n-butyllithium (2.0 mL, 1.0 M THF) over 5 min. The solution was maintained at −78° C. for 1 h. Methylchloroformate (0.80 mL, 10.4 mmol) was then added quickly in a steady stream via syringe. The solution was removed from cooling and allowed to stand at ambient temperature for 1.5 h. The solution was concentrated and purified on silica gel (0-10% ethyl acetate/hexanes, 40 min. gradient) to afford methyl 2-(4-fluorophenyl)-5-methoxybenzo[b]thiophene-3-carboxylate as a yellow residue. 1H NMR (500 MHz, CHLOROFORM-D) δ ppm 7.88 (d, J=2.44 Hz, 1H), 7.66 (d, J=8.85 Hz, 1H), 7.47 (dd, J=8.85, 5.19 Hz, 2H), 7.12 (t, J=8.70 Hz, 2H), 7.05 (dd, J=8.70, 2.59 Hz, 1H), 3.91 (s, 3H), 3.74 (s, 3H). LCMS: retention time: 3.355 min. LC data was recorded on a Shimadzu LC-10AS liquid chromatograph equipped with a Phenomenex-Luna, 10 micron, C18, 4.6×50 mm column using a SPD-10AV UV-Vis detector at a detector wave length of 220 nM. The elution conditions employed a flow rate of 4 mL/min, a gradient of 100% solvent A/0% solvent B to 0% solvent A/100% solvent B, a gradient time of 4 min, a hold time of 1 min, and an analysis time of 5 min where solvent A was 5% CH3CN/95% H2O/10 mM ammonium acetate and solvent B was 5% H2O/95% CH3CN/10 mM ammonium acetate. MS data was determined using a Micromass Platform for LC in electrospray mode. m/z 317 (MH+).

Workup

  1. customThe solution was removed
  2. temperaturefrom cooling
  3. concentrationThe solution was concentrated
  4. custompurified on silica gel (0-10% ethyl acetate/hexanes, 40 min. gradient)

Sources & evidence

ORD record
ord-b2ebdc0544024750993f5262e88af655
Source dataset
uspto-grants-2012_06
Patent number
US08198449B2

Reaction notes

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