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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667274Generated: October 31, 2026

3-Fluoro-4-(trifluoromethyl)benzaldehyde → HCID 45274410, compound

https://huagongshe.com/reaction/1667274

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-4-(trifluoromethyl)benzaldehydeHCID 2737537—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 53391428HCID 53391428—
CatalystAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 45274410HCID 45274410—

Reaction Steps

To a solution of N-azetidin-3-yl-2-[3,3-bis(4-fluorophenyl)-2-oxopyrrolidin-1-yl]acetamide (0.083 g, 0.215 mmol; Example 239A) in dichloromethane (5 mL) was added 3-fluoro-4-(trifluoromethyl)benzaldehyde (0.062 g, 0.323 mmol), sodium triacetoxyborohydride (0.088 g, 0.323 mmol) and a few drops of acetic acid. The reaction mixture was stirred at ambient temperature for 16 hours. The mixture was then diluted with dichloromethane and washed with saturated aqueous NaHCO3 solution. The separated organic layer was dried over MgSO4, concentrated, and purified by silica gel flash chromatography eluting with 5-10% methanol/dichloromethane. 1H NMR (300 MHz, CDCl3) δ ppm 7.54 (t, J=7.6 Hz, 1H), 7.28-7.33 (m, 4H), 7.12-7.16 (m, 2H), 6.98-7.05 (m, 4H), 6.30-6.37 (m, 1H), 4.40-4.59 (m, 1H), 3.99 (s, 2H), 3.54-3.66 (m, 4H), 3.50 (t, J=6.5 Hz, 2H), 2.77 (t, J=6.4 Hz, 4H); MS (ESI+) m/z 562 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044069B2
Source datasetuspto-grants-2011_10
ORD IDord-5ce951c2ffa24cbba71eea8d0b157808
Source noteuspto-grants-2011_10