Ethanol → 2-(3,3-Difluoro-1-methylcyclobutyl)acetic acid

HRID 920746Notes

Reaction equation

HRID 920746 reaction equation
[F:1][C:2]1([F:10])[CH2:5][C:4](CC#N)([CH3:6])[CH2:3]1.[OH-:11].[Na+].[CH2:13]([OH:15])[CH3:14]>O>[F:1][C:2]1([F:10])[CH2:5][C:4]([CH2:14][C:13]([OH:11])=[O:15])([CH3:6])[CH2:3]1

Participants

5

Conditions

Temperature
90 °C

Procedure

To a solution of Intermediate 229C (100 mg, 0.689 mmol) in ethanol (1 mL) and H2O (1 mL) was added a 10% aq. solution of NaOH (2 mL, 0.689 mmol) and the reaction mixture was stirred at 90° C. for 12 h. The reaction mixture was concentrated and the pH of the residue was adjusted to 4 with an aqueous solution of 1.5 N HCl, and the compound was extracted with EtOAc (3×10 mL). The combined organic layer was dried on Na2SO4, filtered and the filtrate evaporated under reduced pressure to afford Intermediate 229D as a yellow sticky liquid (80 mg, 71%). The crude intermediate was taken as such for further reaction without purification. 1H NMR (400 MHz, DMSO-d6) δ ppm 12.14 (brs, 1H), 2.11-2.39 (m, 6H), 1.15 (s, 3H).

Workup

  1. concentrationThe reaction mixture was concentrated
  2. extractionthe compound was extracted with EtOAc (3×10 mL)
  3. customThe combined organic layer was dried on Na2SO4
  4. filtrationfiltered
  5. customthe filtrate evaporated under reduced pressure

Sources & evidence

ORD record
ord-6068457c874c421c8fd7393eae6b48bf
Source dataset
uspto-grants-2016_03
Patent number
US09273058B2

Reaction notes

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