HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfamic Acid → HCID 57443657, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfamic Acid | HCID 5987 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Methylene-3,4-dihydro-2H-1,5-benzodioxepin | HCID 595450 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57443657 | HCID 57443657 | — |
Reaction Steps
3-Methylene-3,4-dihydro-2H-benzo[b][1,4]dioxepine (5.00 g, 30.8 mmol) was dissolved in dry THF (100 mL). Borane-THF (1.0 M in THF, 10.3 mL) was added at 0° C. The reaction was stirred at RT for 5 hours. Aminosulfonic acid (6.97 g, 61.6 mmol) was added. The reaction was heated to reflux overnight. The reaction was cooled to room temperature and aqueous sodium hydroxide (3.0 M, 100 mL) was added. The solution was extracted with ethyl acetate (3×100 mL). The combined organic solution was dried over MgSO4. The solution was concentrated under vacuum and purified by chromatography (2% to 8% methanol in dichloromethane) to yield ((3,4-dihydro-2H-benzo[b][1,4]dioxepin-3-yl)methyl)amine as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084490B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-0d847b1147f24373901713dc66032e3a |
| Source note | uspto-grants-2011_12 |