HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508724Generated: October 25, 2026
4-Aminobenzenepropanol → HCID 74221498, compound
https://huagongshe.com/reaction/1508724
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Aminobenzenepropanol | HCID 220424 | — |
| Reactant | HCID 90111613 | HCID 90111613 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 74221498 | HCID 74221498 | 35.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221843B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-5d60009078ae45ffa621d7e40dd16487 |
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| Source note | uspto-grants-2015_12 |
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