HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Acetic Acid → HCID 178482015, compound

HRID 67698
Notes
Print preview

Reaction equation

HRID 67698 reaction equation
CC(O[CH2:5][C:6]1[CH2:15][S:14][C@@H:9]2[C@H:10]([NH2:13])[C:11](=[O:12])[N:8]2[C:7]=1[C:16]([OH:18])=[O:17])=O.CN1C(C[N:26]2[C:30]([SH:31])=[N:29][N:28]=[N:27]2)=NN=N1.[C:32](O)(=O)[CH3:33].B(F)(F)F.CCOCC>O>[NH2:13][CH:10]1[C:11](=[O:12])[N:8]2[C:7]([C:16]([OH:18])=[O:17])=[C:6]([CH:5]([S:31][C:30]3[NH:29][N:28]=[N:27][N:26]=3)[CH2:33][C:32]3[N:26]([CH3:30])[N:27]=[N:28][N:29]=3)[CH2:15][S:14][C@H:9]12
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 8000Boron trifluoride etherateHCID 4413287-Aminocephalosporanic acidHCID 178482016HCID 178482016, compound

Product 1

HCID 178482015HCID 178482015, compoundYield 80%

Reagents, catalysts & solvents 1

HCID 962
Water
Solvent
2×

Procedure

A solution of 1.54 g. of 7-aminocephalosporanic acid and 1.0 g. (5 mmole) of 1-(1-methyl-1H-tetrazol-5-ylmethyl)-1H-tetrazol-5-thiol in 7.0 ml. of glacial acetic acid was heated in an oil bath to a temperature of about 65°-70° C. To the hot reaction mixture were added 3.6 ml. of boron trifluoride etherate, and the reaction mixture was heated at a temperature of 65°-70° C. for one hour with stirring. The reaction mixture was then cooled to room temperature and 10 ml. of water were added. The reaction mixture was stirred for 15 minutes after water addition, was filtered, and then chilled in an ice bath. The pH of the cold mixture was adjusted to pH 4.5 with concentrated ammonium hydroxide. The precipitate which formed was filtered, washed repeatedly with water, with acetone, and finally with diethyl ether. The off-white solid product was vacuum dried for one hour at 40° C. There was obtained 1.5 g. (80% yield) of the title compound.

Workup

  1. additionTo the hot reaction mixture were added 3.6 ml
  2. stirringThe reaction mixture was stirred for 15 minutes
  3. filtrationwas filtered
  4. temperaturechilled in an ice bath
  5. customThe precipitate which formed
  6. filtrationwas filtered
  7. washwashed repeatedly with water, with acetone
  8. customdried for one hour at 40° C
  9. customThere was obtained 1.5 g

Sources & evidence

ORD record
ord-c828cb921753496e9f48c31b62f15f2f
Source dataset
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04346076

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes