Hydrochloric Acid → HCID 66643896, compound

HRID 1187034Notes

Reaction equation

HRID 1187034 reaction equation
[Br:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:9]Br.C(OC)(=O)[CH2:12][C:13]([O:15]C)=[O:14].[H-].[Na+].Cl>>[Br:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:9][CH2:12][C:13]([OH:15])=[O:14]

Participants

5

Conditions

Temperature
0 °C

Procedure

To a flask charged with 2-bromo-1-(bromomethyl)-3-fluorobenzene (2.0 g, 7.5 mmol) and a stir bar was added dimethyl malonate (20.0 mL, 174 mmol). The solution was cooled to 0° C. in an ice bath. To this solution was carefully added sodium hydride (0.597 g, 14.9 mmol) in small portions. When the addition was done, the reaction was kept stirring for another 30 minutes. The reaction was quenched with NH4Cl, extracted with EtOAc, washed with brine, dried over Na2SO4, and concentrated. The residue was dissolved in acetic acid (50 mL). To this solution was added HCl (50 ml, 330 mmol), and the reaction was heated to reflux for 16 hours. Analysis by LC showed formation of the desired acid. Most of the solvent was removed on a rotary evaporator. The remaining solution was diluted with 50 mL of water, and extracted with ether (50 mL×3). The extracts were combined, and washed with 1N NaOH (50 mL×2). At that point, all the acid was in the aqueous as the salt. The aqueous washes were combined, acidified, and back extracted with DCM (100 mL×2). The extracts were combined, dried over Na2SO4, and concentrated to afford 3-(2-bromo-3-fluorophenyl)propanoic acid.

Workup

  1. additionWhen the addition
  2. customThe reaction was quenched with NH4Cl
  3. extractionextracted with EtOAc
  4. washwashed with brine
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated
  7. dissolutionThe residue was dissolved in acetic acid (50 mL)
  8. temperaturethe reaction was heated
  9. temperatureto reflux for 16 hours
  10. customMost of the solvent was removed on a rotary evaporator
  11. additionThe remaining solution was diluted with 50 mL of water
  12. extractionextracted with ether (50 mL×3)
  13. washwashed with 1N NaOH (50 mL×2)
  14. extractionback extracted with DCM (100 mL×2)
  15. dry with materialdried over Na2SO4
  16. concentrationconcentrated

Sources & evidence

ORD record
ord-9664178bf7dd4000a1cc87997c6a1ffd
Source dataset
uspto-grants-2014_03
Patent number
US08673920B2

Reaction notes

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