Methyl chloroformate → HCID 19788089, compound

HRID 654127Notes

Reaction equation

HRID 654127 reaction equation
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:10]([C:15]([OH:17])=O)=[CH:11][CH:12]=[CH:13][CH:14]=2)=[CH:5][CH:4]=1)[CH3:2].C(N(CC)CC)C.ClC(OC)=O.[N-:30]=[N+:31]=[N-:32].[Na+]>CN(C=O)C.O>[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:10]([C:15]([N:30]=[N+:31]=[N-:32])=[O:17])=[CH:11][CH:12]=[CH:13][CH:14]=2)=[CH:5][CH:4]=1)[CH3:2]

Participants

7

Procedure

To 4'-ethylbiphenylcarboxylic acid (20 mmol) dissolved in 50 mL dry DMF was added 25 mmol of triethylamine and the mixture was cooled in an ice bath, added 38.5 mmol of methyl chloroformate dropwise at 0°-5° C., and then stirred at room temperature for 15 minutes. The mixture was cooled to 0° C. again, and a cold solution of 38.5 mmol of sodium azide dissolved in a minimum amount of water (<8 mL) was added as rapidly as possible (in one portion if possible) at <5° C. The reaction mixture was stirred at 0° C. for 1 hour and poured into 500 mL of ice-water. The resulting precipitate was filtered while still cold (<10 min), washed with cold water and dried under a stream of nitrogen to give the crude 4'-ethylbiphenylcarbonyl azide. The azide was used in place of 4'-ethylbiphenylisocyanate for the subsequent reactions according to the procedures exactly paralleling those described previously for Examples 1 through 3 to give the desired product as a colorless solid, mp 223°-224° C.

Workup

  1. temperaturethe mixture was cooled in an ice bath
  2. temperatureThe mixture was cooled to 0° C. again
  3. additionwas added as rapidly as possible (in one portion if possible) at <5° C
  4. stirringThe reaction mixture was stirred at 0° C. for 1 hour
  5. filtrationThe resulting precipitate was filtered while still cold (<10 min)
  6. washwashed with cold water
  7. customdried under a stream of nitrogen

Sources & evidence

ORD record
ord-8e3d0374501c40daa0db04fad5b2e4ed
Source dataset
uspto-grants-1992_07
Patent number
US05130316

Reaction notes

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