HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927502Generated: November 3, 2026
4-(Trifluoromethyl)benzaldehyde → HCID 131728484, compound
https://huagongshe.com/reaction/1927502
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Trifluoromethyl)benzaldehyde | HCID 67996 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 4-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 ester | HCID 11541072 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131728484 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183234B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-28eef7bafdbe4ebc992a344c35016dc5 |
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| Source note | uspto-grants-2012_05 |
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