HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983474Generated: October 30, 2026
1,1-Dichloroethane → (7-Methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amine hydrochloride
https://huagongshe.com/reaction/983474
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Propylamine | HCID 7852 | — |
| Reactant | 7-Methoxy-2-tetralone | HCID 77785 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Product | (7-Methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amine hydrochloride | HCID 69746401 | — |
Reaction Steps
To a solution of 7-methoxy-3,4-dihydro-1H-naphthalen-2-one (6.0 g, 39.7 mmol) in dichloroethane (130 mL) under an inert atmosphere was added propylamine (3.4 mL, 41.7 mmol, 1.05 eq) followed by sodium triacetoxyborohydride (21 g, 99.3 mmol, 2.5 eq) in a single portion. The reaction was allowed to stir at room temperature for 24 h. The mixture was concentrated in vacuo and partitioned between EtOAc (200 mL) and 5% aq. NaOH (100 mL). The aqueous layer was extracted twice more with EtOAc (2×70 mL). The combined organic layers were washed with brine (100 mL), dried over MgSO4, filtered, and concentrated. The residue was taken up in ether (125 mL) and treated with 1N HCl in ether. The salt was filtered and dried to afford (7-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amine hydrochloride as a tan solid (5.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06864266B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-031654c8fffd4f5380c1524e93ee2de8 |
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| Source note | uspto-grants-2005_03 |
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