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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534216Generated: October 30, 2026

Methyl 4-Formylbenzoate → HCID 86708264, compound

https://huagongshe.com/reaction/534216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-FormylbenzoateHCID 15294—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86708263HCID 86708263—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 86708264HCID 8670826458.7%

Reaction Steps

To a solution of 2,2,2-trifluoro-N-(trans-2-(4-(1-methyl-1H-pyrazol-4-yl)phenyl)cyclopropyl)-N-(piperidin-4-ylmethyl)acetamide (85 mg, 0.209 mmol) in 1,2-dichloroethane (DCE) (2 mL) were added methyl 4-formylbenzoate (41.2 mg, 0.251 mmol) and sodium triacetoxyborohydride (75 mg, 0.356 mmol), and the mixture was stirred at room temperature for 18 h. The mixture was quenched with water (3 mL) and extracted with DCM (3×). The extract was dried (Na2SO4) and concentrated. The residue was purified using column chromatography (silica gel, 0 to 100% EtOAc/hexanes) to give 68 mg of product as off-white solid. MS: (M+H)+=555.3. 1H NMR (400 MHz, METHANOL-d4) δ ppm 1.28-1.53 (m, 4H), 1.56-1.76 (m, 3H), 1.80-1.96 (m, 1H), 1.98-2.11 (m, 3H), 2.44 (br. s., 1H), 2.75-2.97 (m, 3H), 3.09-3.19 (m, 1H), 7.12 (d, J=8.08 Hz, 2H), 7.41-7.55 (m, 5H), 7.91-8.03 (m, 3H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853408B2
Source datasetuspto-grants-2014_10
ORD IDord-fafb7631c51245dabff305b450fffc8b
Source noteuspto-grants-2014_10