HCID 21489517, compound → HCID 21489511, compound

HRID 1579496Notes

Reaction equation

HRID 1579496 reaction equation
Cl[C:2]1[C:7]([O:8][CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:6][C:5]([Cl:15])=[CH:4][N:3]=1>C(O)(=O)C>[CH2:13]([O:12][C:10](=[O:11])[CH2:9][O:8][C:7]1[CH:2]=[N:3][CH:4]=[C:5]([Cl:15])[CH:6]=1)[CH3:14]

Participants

3

Procedure

A solution of ethyl (2,5-dichloropyrid-3-yloxy)-acetate (200mg.) in glacial acetic acid (8ml.) was stirred overnight under reflux with acid washed zinc powder (1.0g.). The solution was cooled and filtered and the filtrate was evaporated to dryness. The residue was purified by chromatography on silica gel to yield ethyl(5-chloropyrid-3-yloxy)acetate, m.p. 38°-40°C. (ether-pentane).

Workup

  1. temperatureunder reflux with acid
  2. washwashed zinc powder (1.0g.)
  3. temperatureThe solution was cooled
  4. filtrationfiltered
  5. customthe filtrate was evaporated to dryness
  6. customThe residue was purified by chromatography on silica gel

Sources & evidence

ORD record
ord-9187f73aed3e428b8410e5cc56542ea6
Source dataset
uspto-grants-1976_01
Patent number
US03931206

Reaction notes

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