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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508724Generated: October 25, 2026

4-Aminobenzenepropanol → HCID 74221498, compound

https://huagongshe.com/reaction/1508724

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminobenzenepropanolHCID 220424—
ReactantHCID 90111613HCID 90111613—
SolventAcetic AcidHCID 176—
SolventSodium BicarbonateHCID 516892—
ProductHCID 74221498HCID 7422149835.4%

Reaction Conditions

Temperature75 °C

Reaction Steps

2-Chloro-4-(3-chlorophenyl)-6-ethyl-1,3,5-triazine (0.150 g, 0.59 mmol) and 3-(4-aminophenyl)propan-1-ol (0.130 g, 0.89 mmol) were suspended in acetic acid (5 mL). The mixture was heated to 75° C. for 2 h. After this time, the reaction was cooled, diluted with saturated aqueous sodium bicarbonate, and extracted with ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated. The residue was purified by column chromatography (silica, hexanes/ethyl acetate) to afford the title compound (0.077 g, 35%) as a yellow solid. MW=368.86. 1H NMR (DMSO-d6, 500 MHz) δ 10.19 (s, 1H), 8.41-8.31 (m, 2H), 7.71-7.67 (m, 3H), 7.60 (t, J=8.0 Hz, 1H), 7.24-7.16 (m, 2H), 4.45 (t, J=5.5 Hz, 1H), 3.43 (q, J=5.5 Hz, 2H), 2.77 (q, J=7.5 Hz, 2H), 2.60 (t, J=7.5 Hz, 2H), 2.51-2.49 (m, 2H), 1.75-1.69 (m, 2H), 1.32 (t, J=7.5 Hz, 3H); APCI MS m/z 369 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221843B2
Source datasetuspto-grants-2015_12
ORD IDord-5d60009078ae45ffa621d7e40dd16487
Source noteuspto-grants-2015_12