Sodium Carbonate → HCID 22730862, compound

HRID 1785756Notes

Reaction equation

HRID 1785756 reaction equation
Br[C:2]1[S:3][C:4]([Cl:7])=[CH:5][CH:6]=1.OB(O)[C:10]1[CH:18]=[CH:17][C:13]([C:14]([OH:16])=[O:15])=[CH:12][CH:11]=1.C([O-])([O-])=O.[Na+].[Na+]>COCCOC.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[Cl:7][C:4]1[S:3][CH:2]=[CH:6][C:5]=1[C:10]1[CH:18]=[CH:17][C:13]([C:14]([OH:16])=[O:15])=[CH:12][CH:11]=1

Participants

6

Conditions

Temperature
75 °C

Procedure

Solid Pd(PPh3)4 (11.0 mg, 0.01 mmol) was treated with a room temperature solution of 2-bromo-5-chlorothiophene (143 mg, 0.72 mmol) in DME (4 mL), stirred for 5 minutes, treated with a solution of 4-(dihydroxyboryl)benzoic acid (100 mg, 0.60 mmol) in DME (2 mL), and stirred for 5 minutes. The mixture was treated with 2M Na2CO3 (1.5 mL, 3.0 mmol), heated to 75° C., stirred for 18 hours, cooled to room temperature, filtered, triturated with water (3 mL), and concentrated. The concentrate was treated with boiling water (4 mL), filtered through celite, cooled to room temperature, adjusted to pH<7 with HCl, and filtered to provide the desired product. MS (APCI(+)) m/e 239 (M+H)+.

Workup

  1. stirringstirred for 5 minutes
  2. stirringstirred for 18 hours
  3. temperaturecooled to room temperature
  4. filtrationfiltered
  5. customtriturated with water (3 mL)
  6. concentrationconcentrated
  7. additionThe concentrate was treated with boiling water (4 mL)
  8. filtrationfiltered through celite
  9. temperaturecooled to room temperature
  10. filtrationfiltered

Sources & evidence

ORD record
ord-5925a432d0514328b5f46ff766abf8fc
Source dataset
uspto-grants-2009_03
Patent number
US07504512B2

Reaction notes

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