HCID 22120793, compound → HCID 54252789, compound

HRID 1493620Notes

Reaction equation

HRID 1493620 reaction equation
[CH3:1][O:2][C:3](=[O:19])[CH2:4][NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([O:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:7]=1.[N:20]([O-])=O.[Na+]>C(O)(=O)C.O.[Zn]>[O:12]([C:8]1[CH:7]=[C:6]([N:5]([CH2:4][C:3]([O:2][CH3:1])=[O:19])[NH2:20])[CH:11]=[CH:10][CH:9]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

Participants

6

Procedure

N-(3-Phenoxyphenyl)glycine methyl ester (Intermediate 48; 10 g, 0.0389 mol) was dissolved in a mixture of glacial acetic acid (60 ml) and water (7 ml) and the solution was cooled to between 0° and 5° C. A solution of sodium nitrite (2.8 g, 0.0408 mol) in water (8.5 ml) was added to this over 15 min at the same low temperature. The solution was stirred for 1 h before being cooled to between 0° and -10° C. Zinc powder (9.9 g, 0.1517 mol) was gradually added at this temperature and the reaction was then stirred at 0° to 5° C. for 4 h. It was then poured into water (300 ml) and extracted with ethyl acetate (3×150 ml). The organic extract was washed with 8% sodium bicarbonate solution until effervescence had ceased. It was then dried and evaporated to give a dark brown oil. This was purified by FCC on deactivated silica (200 g) eluting with hexane-chloroform (2:1) to give the title compound as a brown oil (2.7 g, 25%).

Workup

  1. temperaturethe solution was cooled to between 0° and 5° C
  2. temperaturebefore being cooled to between 0° and -10° C
  3. stirringthe reaction was then stirred at 0° to 5° C. for 4 h
  4. extractionextracted with ethyl acetate (3×150 ml)
  5. extractionThe organic extract
  6. washwas washed with 8% sodium bicarbonate solution until effervescence
  7. customIt was then dried
  8. customevaporated
  9. customto give a dark brown oil
  10. customThis was purified by FCC on deactivated silica (200 g)
  11. washeluting with hexane-chloroform (2:1)

Sources & evidence

ORD record
ord-31fb00e4b584423c87de2f40760e358f
Source dataset
uspto-grants-1991_06
Patent number
US05023255

Reaction notes

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