Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5768Generated: October 26, 2026

Acetic Acid → 3-(1,2,3,4-Tetrahydronaphthalen-1-YL)-3H-imidazole-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/5768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAmmonium AcetateHCID 517165—
ReactantN,alpha-bis-formyl-N-(1,2,3,4-tetrahydronaphthalen-1-yl)glycine methyl esterHCID 19794118—
SolventWaterHCID 962—
Product3-(1,2,3,4-Tetrahydronaphthalen-1-YL)-3H-imidazole-4-carboxylic acid methyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246915
Source datasetuspto-grants-1993_09
ORD IDord-f57d7a6d780c4a4a823cce69c82616b4
Source noteuspto-grants-1993_09