HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-(5-Bromo-2,3-dihydro-benzofuran-4-yl)-propylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-(2,3-Dihydro-benzofuran-4-yl)-propylamine hydrochloride | HCID 19611670 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-(5-Bromo-2,3-dihydro-benzofuran-4-yl)-propylamine | HCID 19611637 | — |
Reaction Steps
A solution of the free base (200 mg) liberated from 3-(2,3-dihydro-benzofuran-4-yl)-propylamine hydrochloride and N-bromosuccinimide (215 mg) in acetic acid (5 ml) was stirred at room temperature overnight. The solution was evaporated to dryness and the residue taken up in water, basified to pH9-10 with 2N sodium hydroxide and extracted with ethyl acetate. The extracts were dried and evaporated to give the title compound (256 mg) as a pale yellow oil. Tic SiO2 (Dichloromethane/methanol/0.880 ammonia 75:8:1) Rf 0.53
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05981572 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-8162816dff3743df98aae48742dfd4f9 |
| Source note | uspto-grants-1999_11 |