Potassium Fluoride → HCID 57558488, compound

HRID 1724009Notes

Reaction equation

HRID 1724009 reaction equation
[CH3:1][C:2]1([CH3:38])[CH2:11][CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:12](=[O:37])[CH:13](OS(C3C=CC(C)=CC=3)(=O)=O)[C:14]3[CH:19]=[C:18]([O:20][CH3:21])[C:17]([O:22][CH3:23])=[C:16]([O:24][CH3:25])[CH:15]=3)[CH:8]=2)[O:3]1.[F-:39].[K+]>C(#N)C.O>[F:39][CH:10]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:12](=[O:37])[CH2:13][C:14]3[CH:15]=[C:16]([O:24][CH3:25])[C:17]([O:22][CH3:23])=[C:18]([O:20][CH3:21])[CH:19]=3)[CH:8]=2)[O:3][C:2]([CH3:1])([CH3:38])[CH2:11]1

Participants

5

Conditions

Temperature
90 °C

Procedure

To a solution of toluene-4-sulfonic acid 2-(2,2-dimethyl-chroman-6-yl)-2-oxo-1-(3,4,5-trimethoxy-phenyl)-ethyl ester (21.6 mg, 0.04 mmol) in anhydrous ACN (0.5 mL) is added KF (4.72 mg, 0.08 mmol) and Kryptofix (30.6 mg, 0.08 mmol). After completion of addition the reaction mixture is heated to 90° C. After 15 minutes, the reaction mixture is cooled down to room temperature and diluted with water. The aqueous layer is separated and extracted with ethyl acetate (3×). All combined organic layers are dried over Na2SO4, filtered, and concentrated to yield an oil. The crude material is purified using reverse phase to yield the desired compound.

Workup

  1. additionAfter completion of addition the reaction mixture
  2. temperaturethe reaction mixture is cooled down to room temperature
  3. customThe aqueous layer is separated
  4. extractionextracted with ethyl acetate (3×)
  5. dry with materialAll combined organic layers are dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto yield an oil
  9. customThe crude material is purified

Sources & evidence

ORD record
ord-62a88ef8cfe74a2b8774b072c140feda
Source dataset
uspto-grants-2009_02
Patent number
US07485283B2

Reaction notes

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