HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725362Generated: November 2, 2026
1-Tetralone → N-(3,4-dihydro-2H-naphthalen-1-ylidene)hydroxylamine
https://huagongshe.com/reaction/1725362
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Tetralone | HCID 10724 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(3,4-dihydro-2H-naphthalen-1-ylidene)hydroxylamine | HCID 76876 | 63.9% |
Reaction Steps
Add hydroxylamine hydrochloride (71.0 g, 1.03 mol) to a solution of α-tetralone (100.0 g, 0.68 mol) in 300 mL of methanol and stir the resulting solution at reflux for 2 hours. Cool the mixture to 20-24° C. and concentrate under reduced pressure. Dilute the residue with 1 L of water and extract with dichloromethane. Wash the organic layer with saturated aqueous sodium chloride, dry over sodium sulfate, filter, and concentrate under reduced pressure. Crystallize the residue from isopropanol to provide the desired compound as an off-white solid (70.0 g, 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07491716B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-7e05f2a32a9e4ca2b04a3ae1ffeae1c4 |
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| Source note | uspto-grants-2009_02 |
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