Water → HCID 67226454, compound

HRID 2273802Notes

Reaction equation

HRID 2273802 reaction equation
[O:1]1[C:5]2([CH2:10][CH2:9][NH:8][CH2:7][CH2:6]2)[O:4][CH2:3][CH2:2]1.F[C:12]1[CH:21]=[CH:20][C:15]([C:16]([O:18][CH3:19])=[O:17])=[C:14]([O:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH:13]=1.C([O-])([O-])=O.[K+].[K+].O>CS(C)=O>[O:22]([C:14]1[CH:13]=[C:12]([N:8]2[CH2:9][CH2:10][C:5]3([O:4][CH2:3][CH2:2][O:1]3)[CH2:6][CH2:7]2)[CH:21]=[CH:20][C:15]=1[C:16]([O:18][CH3:19])=[O:17])[C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1

Participants

6

Procedure

1,4-dioxa-8-azaspiro[4.5]decane (1.18 g), methyl 4-fluoro-2-phenoxybenzoate (1.85 g), and K2CO3 (1.14 g) was stirred at 125° C. in dimethylsulfoxide (25 mL) for 24 hours. The mixture was cooled, poured into 300 mL water, extracted three times with ether, and the ether extracts were combined, rinsed three times with water, and brine, and concentrated. The residue was chromatographed on silica gel using 10-30% ethyl acetate in hexanes as eluent to give the title compound.

Workup

  1. temperatureThe mixture was cooled
  2. extractionextracted three times with ether
  3. washrinsed three times with water, and brine
  4. concentrationconcentrated
  5. customThe residue was chromatographed on silica gel using 10-30% ethyl acetate in hexanes as eluent

Sources & evidence

ORD record
ord-71a74ee74d8c4209b5601d1163e0b77d
Source dataset
uspto-grants-2015_09
Patent number
US09125913B2

Reaction notes

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