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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742322Generated: October 26, 2026

2-Phenylbutyric Acid → Methyl 3-methoxy-4-[6-(2-phenylbutanamido)benzimidazol-1-ylmethyl]benzoate

https://huagongshe.com/reaction/1742322

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Phenylbutyric AcidHCID 7012—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantMethyl 4-(6-aminobenzimidazol-1-ylmethyl)-3-methoxybenzoateHCID 14763098—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-methoxy-4-[6-(2-phenylbutanamido)benzimidazol-1-ylmethyl]benzoateHCID 2336589125%

Reaction Steps

A solution of 1,1'-carbonyldiimidazole (0.23 g.) and 2-phenylbutyric acid (0.22 g.) in dichloromethane (3 ml.) was heated under reflux for 30 minutes and then treated with a solution of (J) (0.41 g.) in dichloromethane (3 ml.). The mixture was heated under reflux for an additional 10 minutes and then diluted with dichloromethane. This mixture was washed successively with 10% v/v hydrochloric acid, water, and brine, then dried (MgSO4) and evaporated. The resultant residue was purified by flash chromatography on a 5×25 cm. silica gel column using 3:97 v/v methanol:dichloromethane as the eluent to give the title compound (0.15 g., 25%): partial NMR: 2.0(br m,2H, CH3CH2), 3.4(t,1H, CH2CH), 7.3(s,5H, Ar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05338734
Source datasetuspto-grants-1994_08
ORD IDord-3f4aa721cf3e4b968a66501ddc3e4a38
Source noteuspto-grants-1994_08