Sodium Carbonate → HCID 69838792, compound

HRID 2083914Notes

Reaction equation

HRID 2083914 reaction equation
[C:1](=[O:4])([O-])[O-:2].[Na+].[Na+].[Cl:7][C:8]1[CH:9]=[C:10]2[C:15](=[C:16]([O:18][CH:19]([F:21])[F:20])[CH:17]=1)[S:14][CH2:13][CH2:12][C@:11]2([OH:24])CO>O.[Pt]>[Cl:7][C:8]1[CH:9]=[C:10]2[C:15](=[C:16]([O:18][CH:19]([F:20])[F:21])[CH:17]=1)[S:14][CH2:13][CH2:12][C@@:11]2([C:1]([OH:2])=[O:4])[OH:24]

Participants

5

Conditions

Temperature
95 °C

Procedure

Sodium carbonate (0.72 g, 6.7 mmol) and 5% Pt/C (1.50 g, 75% weight of reactant) were added to a solution of (R)-6-chloro-8-difluoromethoxy-4-hydroxy-4-hydroxymethylthiochromane (2.0 g, 6.7 mmol; from step (v) above) in H2O (180 mL). The mixture was vigorously stirred at ca. 95° C. for 20-40 h with air being directly bubbled into the reaction mixture. The reaction was cooled to room temperature and filtered through a pad of Celite with saturated Na2CO3 solution (ca. 100 mL). The resulting liquid was slowly acidified with 2 N HCl (ca. 200 mL) and extracted with EtOAc (2×100 mL). The combined organic layers were washed with brine (75 mL), dried (Na2SO4), filtered, and concentrated in vacuo to afford 1.56 g (ca. 75%) of the sub-title compound as a brown oil which was used without further purification.

Workup

  1. custombeing directly bubbled into the reaction mixture
  2. temperatureThe reaction was cooled to room temperature
  3. filtrationfiltered through a pad of Celite with saturated Na2CO3 solution (ca. 100 mL)
  4. extractionextracted with EtOAc (2×100 mL)
  5. washThe combined organic layers were washed with brine (75 mL)
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-0c481ca978344454ba3f7dafccb4dc4b
Source dataset
uspto-grants-2004_04
Patent number
US06716834B2

Reaction notes

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