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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529351Generated: October 31, 2026

4-Formylbenzoic acid → HCID 68385262, compound

https://huagongshe.com/reaction/529351

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Formylbenzoic acidHCID 12088—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86708247HCID 86708247—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 68385262HCID 6838526262.1%

Reaction Steps

To a solution of 2,2,2-trifluoro-N-(trans-2-phenylcyclopropyl)-N-(2-(piperidin-4-yl)ethyl)acetamide (126 mg, 0.370 mmol) in 1,2-dichloroethane (DCE) (2 mL) were added 4-formylbenzoic acid (66.7 mg, 0.444 mmol) and sodium triacetoxyborohydride (157 mg, 0.740 mmol), and the mixture was stirred at room temperature for 18 h. The mixture was quenched with water (2 mL) and extracted with DCM (3×). The extract was dried (Na2SO4) and concentrated. The residue was dissolved into methanol (2 ml) and 1N NaOH aqueous solution (2 mL) was added. The mixture was stirred at room temperature for 1 h and concentrated. The residue was treated with MeOH (3 mL) and filtered. The filtrate was purified using reverse-phase HPLC under the acidic conditions. The resulting TFA salt of the product was treated with 1N HCl and concentrated. The residue was further dried under vacuum to give 87 mg of product as white solid (HCl salt). MS: (M+H)+=379.4. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.25 (q, 1H), 1.46-1.67 (m, 5H), 1.82 (br. s., 2H), 2.87 (br. s., 3H), 3.05 (br. s., 2H), 3.30 (br. s., 2H), 4.34 (d, J=3.79 Hz, 2H), 7.10-7.40 (m, 5H), 7.74 (d, J=8.08 Hz, 2H), 8.00 (d, J=7.83 Hz, 2H), 9.53 (br. s., 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346840B2
Source datasetuspto-grants-2016_05
ORD IDord-fb3f873e71ec4a949730b262cb050c83
Source noteuspto-grants-2016_05