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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220145Generated: October 29, 2026

Ethyl 3-aminobenzoate → HCID 1722082, compound

https://huagongshe.com/reaction/2220145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-aminobenzoateHCID 11400—
ReactantValeryl chlorideHCID 61186—
ReactantSodium BicarbonateHCID 516892—
SolventDimethylacetamideHCID 31374—
ProductHCID 1722082HCID 1722082—

Reaction Steps

To a solution of ethyl 3-aminobenzoate (5.02 g) in N,N-dimethylacetamide (DMA, 50 ml) was added dropwise pentanoyl chloride (4.0 ml), and the mixture was stirred at room temperature for 1 hr. Saturated aqueous sodium hydrogencarbonate was added to the reaction mixture, and the mixture was stirred for 1 hr. The mixture was partitioned and extracted by adding ethyl acetate, and the extract was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated to give ethyl 3-(N-pentanoyl)aminobenzoate (7.55 g). To a solution of the obtained amide compound in DMA (100 ml) was added potassium tert-butoxide (4.09 g), and the mixture was stirred for 30 min. To the reaction mixture was added [4-[2-(3-triphenylmethyl-3H-tetrazol-5-yl)phenyl]phenyl]methylbromide (18.6 g), and the mixture was stirred at 50° C. for 3 hrs. The reaction mixture was added to ethyl acetate-water and, after partitioning and extraction, the extract was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel column chromatography (eluted with hexane-ethyl acetate:3-2 v/v) to give the object compound (20.6 g, yield 93.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417052B2
Source datasetuspto-grants-2008_08
ORD IDord-ec9c91a2f65a41c0a7279106bea86146
Source noteuspto-grants-2008_08