HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220145Generated: October 29, 2026
Ethyl 3-aminobenzoate → HCID 1722082, compound
https://huagongshe.com/reaction/2220145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 3-aminobenzoate | HCID 11400 | — |
| Reactant | Valeryl chloride | HCID 61186 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 1722082 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07417052B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-ec9c91a2f65a41c0a7279106bea86146 |
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| Source note | uspto-grants-2008_08 |
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