HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242934Generated: November 1, 2026
Sodium borohydride → HCID 21939779, compound
https://huagongshe.com/reaction/1242934
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57373319 | HCID 57373319 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21939779 | HCID 21939779 | 45.7% |
Reaction Steps
The obtained 6-acetamido-2-(N,N-dimethylaminomethylidene)-1-tetralone (4.50 g, 0.0173 mol) was dissolved in methanol (50 ml), and sodium borohydride (6.56 g, 0.173 mol) was added to the solution under ice-cooling, which was stirred for 2 hours. The reaction mixture was concentrated. Ethyl acetate and sodium hydrogencarbonate solution were added to the residue, and extraction was conducted. The ethyl acetate layer was concentrated, and 30 ml of tetrahydrofuran and 30 ml of 2N hydrochloric acid were added to the residue, which was refluxed with heating for 16 hours. The reaction mixture was concentrated, and ethyl acetate and 2N sodium hydroxide solution were added, and extraction was conducted. The ethyl acetate layer was concentrated, and the residue was refined using alumina column chromatography (development solvent; ethyl acetate:n-hexane=30:70), to give 6-[(N,N-dimethylamino)methyl]-7,8-dihydro-2-naphthaleneamine (1.60 g) as a colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07115750B1 |
|---|
| Source dataset | uspto-grants-2006_10 |
|---|
| ORD ID | ord-e34d1536105641398c0fa90fe9213d75 |
|---|
| Source note | uspto-grants-2006_10 |
|---|