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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31739Generated: October 23, 2026

Trifluoroacetic acid → 4-acetyl-N-(3-methoxybenzyl)benzamide

https://huagongshe.com/en/reaction/31739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-MethylmorpholineHCID 7972—
Reactant4-Acetylbenzoic AcidHCID 11470—
Reactant3-MethoxybenzylamineHCID 21156—
ReactantPyBOPHCID 2724699—
SolventDichloromethaneHCID 6344—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-acetyl-N-(3-methoxybenzyl)benzamideHCID 5984089597%

Reaction Steps

The Sasrin resin was prepared as described in Step 2 of Example 3. The resin (500 mg) was heated with a solution of 3-methoxybenzylamine (600 μl ) in NMP (6 ml) at 70° C. for 4 hours. The resin was then washed with DMF and dichloromethane and then shaken with a solution of PyBop® (1.04 g, 2 mmol), 4-acetylbenzoic acid (0.33 g, 2 mmol), 4-methylmorpholine (4 mmol) in NMP (6 ml) at room temperature overnight. A small aliquot of the resin was treated with 20% TFA in dichloromethane to give the intermediate, (4-acetylphenyl)-N-[(3-methoxyphenyl)methyl]carboxamide (HPLC: 23.94 min (97%); MS; MH+=284 (as required)). The resin was then heated at 95° C. for 7 hours in DMFDMA (5 ml).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425557B2
Source datasetuspto-grants-2008_09
ORD IDord-1818aeeacb4c4b8996cc79a60014620c
Source noteuspto-grants-2008_09