HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357270Generated: October 31, 2026
Hydrochloric Acid → (5-Bromo-6-methoxy-naphthalen-2-ylmethyl)-methyl-amine
https://huagongshe.com/reaction/1357270
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (5-Bromo-6-methoxy-naphthalen-2-ylmethylene)-methyl-amine | HCID 18505272 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (5-Bromo-6-methoxy-naphthalen-2-ylmethyl)-methyl-amine | HCID 18505315 | 94% |
Reaction Steps
Sodium borohydride (131 mg, 3.47 mmol) was added under nitrogen to a warm solution of (5-bromo-6-methoxy-naphthalen-2-ylmethylene)-methyl-amine (950 mg, 4.41 mmol), prepared in the previous step, in 30 mL of absolute ethanol. After the addition the reaction was stirred at room temperature for 19 h (overnight). 1 N HCl was added dropwise until the reaction was pH˜1 (litmus paper). The solvent was removed under reduced pressure and the residue partitioned between methylene chloride and water. The aqueous layer was made basic by the addition of 1 N NaOH. The organic layer was separated and the aqueous layer was extracted three times with methylene chloride. The combined extracts were dried (MgSO4) and the solvent removed under reduced pressure to give (5-bromo-6-methoxy-naphthalen-2-ylmethyl)-methyl-amine (900 mg, 94%) as an off-white solid, mp 41-45° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06589970B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-bbceb141f3374b4e85e5c9b7cfdfe4eb |
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| Source note | uspto-grants-2003_07 |
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