HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513894Generated: November 3, 2026
Monobenzone → 4-(2-Azepan-1-yl-ethoxy)-phenol
https://huagongshe.com/reaction/1513894
Participants
| Role | Name | HCID | Charge |
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| Reactant | Monobenzone | HCID 7638 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 2-(hexamethyleneimino)ethyl chloride HCl | HCID 53445277 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(2-Azepan-1-yl-ethoxy)-phenol | HCID 67004800 | 59,879.301% |
Reaction Steps
Add sodium hydride (18 g, 0.45 mol) into a solution of 4-benzyloxylphenol (41 g, 0.20 mol) and 2-(hexamethyleneimino)ethyl chloride hydrochloride (44 g, 0.22 mmol) in THF (600 mL) and DMF (100 mL) at room temperature. Heat to 60° C. for 30 minutes. Pour the solution into ice and water. Dilute with ethyl acetate (500 mL) and separate layers. Dry the organic layer with magnesium sulfate, filter and concentrate under reduced pressure to give brown oil. Dissolve the oil in ethyl acetate (500 mL) and methanol (500 mL). Add ammonium formate (100 g, 1.59 mol) and palladium on carbon (10 g, 9.4 mmol). Heat the mixture to reflux for 30 minutes. Add ammonium formate (100 g, 1.59 mol) and palladium on carbon (10 g, 9.4 mmol). Heat the reaction mixture for 30 minutes. Filter the suspension through a pad of celite and elute with ethyl acetate (500 ml). Evaporate solvent under reduced pressure and add water (100 mL). Dilute the mixture with ethyl acetate (500 mL) and separate layers. Wash the organic layer with saturated sodium bicarbonate solution (2×200 mL), dry with magnesium sulfate, filter and evaporate solvent under reduced pressure to give 31 g (64%) of 4-(2-azepan-1-yl-ethoxy)-phenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08217032B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-ff0643e5278a48b0854db386522f8bef |
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| Source note | uspto-grants-2012_07 |
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