HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4H-1,3-Benzodioxin-2-methanamine, 6-chloro-N-(1-methylethyl)-4-phenyl-, hydrochloride, cis-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diboron | HCID 6328200 | — |
| Reactant | HCID 22799976 | HCID 22799976 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4H-1,3-Benzodioxin-2-methanamine, 6-chloro-N-(1-methylethyl)-4-phenyl-, hydrochloride, cis- | HCID 3049702 | 208.9% |
Reaction Steps
A solution of cis-6-chloro-4-phenyl-N-(2-propyl)-1,3-benzodioxan-2-carboxamide (6.6 g, 20.0 mmoles) in 400 ml of anhydrous THF was treated with 80 ml (80 mmoles) of diborane in THF solution (1M as BH3) and the reaction mixture was worked up essentially as described in Example 5b. The oily amine was converted to the hydrochloride in anhydrous ether; 7.4 g of colorless powder was obtained. Recrystallization from absolute EtOH gave 5.96 g (84%) of colorless crystals; mp 224.5°-225.5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04056540 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-c8f9a85b3d4345dcac53b00d1d28eb9f |
| Source note | uspto-grants-1977_11 |