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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927502Generated: November 3, 2026

4-(Trifluoromethyl)benzaldehyde → HCID 131728484, compound

https://huagongshe.com/reaction/1927502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzaldehydeHCID 67996—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-Chloro-6-methyl-10,10-dioxo-2-piperazin-1-yl-10,11-dihydro-5-oxa-10lambda*6*-thia-dibenzo[a,d]cyclo heptene-8-carboxylic acid methyl esterHCID 11541072—
CatalystTitanium isopropoxideHCID 11026—
SolventMethanolHCID 887—
ProductHCID 131728484HCID 131728484—

Reaction Steps

p-(Trifluoromethyl)benzaldehyde (0.119 g, 0.687 mmol) and titanium isopropoxide (0.26 mL, 0.858 mmol) were added to a suspension of Example 104k (0.3 g, 0.687 mmol) in methanol (30 mL). The reaction mixture was refluxed for 1.5 h, cooled to room temperature, treated with sodium cyanoborohydride (0.042 g, 0.66 mmol) and stirred for 3 h. It was concentrated, treated with water and extracted with n-butanol. The organic layer was washed with water, brine, dried, concentrated and purified using flash chromatography (silica gel, 20% ethyl acetate/pet.ether) to obtain the title compound. Yield: 0.12 g, (28.7%); 1H NMR (DMSO-d6): δ 2.6 (h, 4H, 2CH2), 2.7 (s, 3H, CH3), 3.2 (h, 4H, 2CH2), 3.6 (s, 2H, CH2), 3.9 (s, 3H, OCH3), 4.6 (s, 2H, CH2), 6.7 (s, H, Ar), 6.9 (s, 1H, Ar), 7.5 (d, 2H, Ar), 7.6 (d, 2H, Ar), 8.1 (s, 1H, Ar), 8.45 (s, 1H, Ar); MS: m/e (ES+) 596 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183234B2
Source datasetuspto-grants-2012_05
ORD IDord-28eef7bafdbe4ebc992a344c35016dc5
Source noteuspto-grants-2012_05