HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-(1,2,3,4-Tetrahydronaphthalen-1-YL)-3H-imidazole-4-carboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | N,alpha-bis-formyl-N-(1,2,3,4-tetrahydronaphthalen-1-yl)glycine methyl ester | HCID 19794118 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(1,2,3,4-Tetrahydronaphthalen-1-YL)-3H-imidazole-4-carboxylic acid methyl ester | HCID 14497624 | — |
Reaction Steps
A mixture of 16.5 g of N,α-bis-formyl-N-(1,2,3,4-tetrahydronaphthalen-1-yl) glycine methyl ester, 65.0 g of ammonium acetate and 100 ml of acetic acid are refluxed for 8 hours. Then additional 50 g ammonium acetate are added and the refluxing is continued for further 4 hours. The solution is diluted with 300 ml of water and extracted twice, with 100 ml of toluene each time. The organic phases are combined, concentrated and separated at silica gel by chromatography. Concentration of the eluate yields 1-(1,2,3,4-tetrahydronaphthalen-1-yl) -5-imidazolecarboxylic acid methyl ester, having a melting point of 63° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05246915 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-f57d7a6d780c4a4a823cce69c82616b4 |
| Source note | uspto-grants-1993_09 |