2,3-Difluoro-6-methoxyphenylacetic acid → 2-(2,3-Difluoro-6-methoxyphenyl)ethanol

HRID 921175Notes

Reaction equation

HRID 921175 reaction equation
[F:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[C:4]([O:9][CH3:10])[C:3]=1[CH2:11][C:12](O)=[O:13].[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[F:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[C:4]([O:9][CH3:10])[C:3]=1[CH2:11][CH2:12][OH:13]

Participants

4

Conditions

Temperature
60 °C

Procedure

To a solution of 2-(2,3-difluoro-6-methoxyphenyl)acetic acid (1 g, 4.95 mmol) in THF (20 mL) at 0° C. was added 1M LAH (9.89 mL, 9.89 mmol) in THF and the resulting mixture was heated at 60° C. for 3 h. Mixture was then cooled and quenched with dropwise addition of water (0.5 mL), 1N NaOH (0.5 mL), and then 1 mL H2O. After stirring for 15 min, the mixture was filtered through celite. The filtrate was concentrated in vacuo. The residue was dried under high vacuum to afford 2-(2,3-difluoro-6-methoxyphenyl)ethanol (810 mg, 4.30 mmol, 87% yield) as a clear viscous oil. Used as is in the next step without further purification. 1H NMR (500 MHz, CDCl3) δ 7.01 (q, J=9.2 Hz, 1H), 6.62-6.53 (m, 1H), 3.92-3.75 (m, 5H), 3.00 (td, J=6.6, 1.9 Hz, 2H), 1.65 (t, J=5.7 Hz, 1H).

Workup

  1. temperatureMixture was then cooled
  2. customquenched with dropwise addition of water (0.5 mL), 1N NaOH (0.5 mL)
  3. filtrationthe mixture was filtered through celite
  4. concentrationThe filtrate was concentrated in vacuo
  5. customThe residue was dried under high vacuum

Sources & evidence

ORD record
ord-4bb99150f12f44d09de953b43635a720
Source dataset
uspto-grants-2016_03
Patent number
US09273067B2

Reaction notes

Loading…