Ethyl chloroformate → HCID 12298145, compound

HRID 1448292Notes

Reaction equation

HRID 1448292 reaction equation
[NH:1]([C:8]1([C:14]([OH:16])=[O:15])[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Na].[OH-].[Na+].Cl[C:21]([O:23][CH2:24][CH3:25])=[O:22]>O1CCCC1>[NH:1]([C:8]1([C:14]([OH:16])=[O:15])[CH2:9][CH2:10][N:11]([C:21]([O:23][CH2:24][CH3:25])=[O:22])[CH2:12][CH2:13]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

6

Procedure

To a stirred and cooled (ice-salt bath) mixture of 12.1 parts of 4-anilinoisonipecotic acid, sodium salt, 200 parts of sodium hydroxide solution 1 N and 20 parts of tetrahydrofuran are added dropwise 6.45 parts of ethyl chloroformate in 25 parts of tetrahydrofuran over 15 minutes and at a temperature between 2° and 5° C. Upon completion, stirring is continued for 3 hours in the cool-bath. The whole is extracted with ether. The aqueous phase is separated and degassed on a rotavapor without heating. The mixture is acidified with glacial acetic acid, whereupon an oil is separated. The latter is stirred in fresh water and extracted with chloroform. The extract is washed three times with water, dried, filtered and evaporated. The residue is crystallized from a mixture of ethyl acetate and petroleumether, yielding 4-anilino-1-(ethoxycarbonyl)isonipecotic acid; mp. 149°-156° C.

Workup

  1. temperaturecooled
  2. customat a temperature between 2° and 5° C
  3. stirringUpon completion, stirring
  4. extractionThe whole is extracted with ether
  5. customThe aqueous phase is separated
  6. customdegassed on a rotavapor
  7. temperaturewithout heating
  8. customis separated
  9. stirringThe latter is stirred in fresh water
  10. extractionextracted with chloroform
  11. washThe extract is washed three times with water
  12. customdried
  13. filtrationfiltered
  14. customevaporated
  15. customThe residue is crystallized from a mixture of ethyl acetate and petroleumether

Sources & evidence

ORD record
ord-b61d3b2772654d85a2e3a800a42b2614
Source dataset
uspto-grants-1979_12
Patent number
US04179569

Reaction notes

Loading…