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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931192Generated: November 1, 2026

Ethanol → HCID 74408212, compound

https://huagongshe.com/reaction/1931192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
Reactant2-(1,1,2,2-Tetrafluoroethoxy)benzaldehydeHCID 2778814—
ReactantHCID 57507187HCID 57507187—
SolventCyclohexane ethylacetateHCID 21867204—
ProductHCID 74408212HCID 7440821268%

Reaction Steps

A 10 mL flask was charged with (4-hydrazino-6-morpholin-4-yl-1,3,5-triazin-2-yl)-(4-trifluoromethoxyphenyl)amine (XV) (159 mg, 0.43 mmol), 4-(1,1,2,2-tetrafluoroethoxybenzaldehyde (142 μL, 0.86 mmol), and ethanol (5 mL) and the mixture was stirred at ambient temperature for 24 h. Water (5 mL) was added to the reaction mixture which was then extracted with EtOAc (3×5 mL). The combined organic extract was washed with brine (10 mL), dried over sodium sulfate, filtered, and concentrated under vacuum. Flash chromatography (silica gel, 10% EtOAc/cyclohexane) afforded compound 1 (167 mg, 68% yield): m.p. 203-206° C.; 1H NMR (CDCl3) δ 8.65 (s, 1H), 7.79 (s, 1H), 7.66-7.55 (m, 4H), 7.20-7.12 (m, 4H), 6.10-5.73 (tt, J1=53.1 Hz, J2=2.56 Hz, 1H), 3.86-3.75 (m, 8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188273B2
Source datasetuspto-grants-2012_05
ORD IDord-8ad30c6f230d433386621da140d8ed97
Source noteuspto-grants-2012_05