Potassium Carbonate → HCID 53855288, compound

HRID 1648028Notes

Reaction equation

HRID 1648028 reaction equation
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:18]=[CH:17][C:11]2[C:12](=[O:16])[CH2:13][CH2:14][O:15][C:10]=2[C:9]=1[CH2:19][CH2:20][CH3:21].[CH2:22]([O:24][C:25](=[O:46])[CH2:26][CH2:27][C:28]1[CH:33]=[C:32]([C:34]2[O:35][C:36](=[O:44])[C:37]3[CH:43]=[CH:42][CH:41]=[CH:40][C:38]=3[CH:39]=2)[CH:31]=[CH:30][C:29]=1[OH:45])[CH3:23].C(=O)([O-])[O-].[K+].[K+]>CC(=O)CC>[CH2:22]([O:24][C:25](=[O:46])[CH2:26][CH2:27][C:28]1[CH:33]=[C:32]([C:34]2[O:35][C:36](=[O:44])[C:37]3[CH:43]=[CH:42][CH:41]=[CH:40][C:38]=3[CH:39]=2)[CH:31]=[CH:30][C:29]=1[O:45][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:18]=[CH:17][C:11]2[C:12](=[O:16])[CH2:13][CH2:14][O:15][C:10]=2[C:9]=1[CH2:19][CH2:20][CH3:21])[CH3:23]

Participants

5

Procedure

A mixture of 0.352 g (0.99 mmol) of 7-[(5-bromopentyl)oxy]-2,3-dihydro-8-propyl-4H-1-benzopyran-4-one, 0.346 g (1.02 mmol) of 2-hydroxy-5-(1-oxo-1H-2-benzopyran-3-yl)benzenepropanoic acid ethyl ester, 0.574 g (4.15 mmol) of anhydrous granular potassium carbonate and 20.9 mL of 2-butanone was stirred and refluxed for 45 hrs. The resulting slurry was filtered with suction and the solids were washed thoroughly with ethyl acetate. The filtrate and washes were combined and concentrated in vacuo and the residue was purified by flash chromatography on 75 g of silica gel, eluting with 3:1 hexane-ethyl acetate, affording 0.352 g (58.1%) of the title compound as a white solid, mp 143.5°-144° C.

Workup

  1. temperaturerefluxed for 45 hrs
  2. filtrationThe resulting slurry was filtered with suction
  3. washthe solids were washed thoroughly with ethyl acetate
  4. concentrationconcentrated in vacuo
  5. customthe residue was purified by flash chromatography on 75 g of silica gel
  6. washeluting with 3:1 hexane-ethyl acetate

Sources & evidence

ORD record
ord-97b293df4a87405680b0ef5edcc1c00d
Source dataset
uspto-grants-1995_07
Patent number
US05434186

Reaction notes

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