HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → HCID 18635434, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 67822515 | HCID 67822515 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 18635434 | HCID 18635434 | — |
Reaction Steps
The intermediate cis-N-allyl-5-methoxy-1-methyl-2-(n-propylamino) tetralin hydrochloride (20 mg; 0.68 mmol) was dissolved in CHCl3 (2 ml) and added during 2 minutes to a well-stirred solution of BBr3 (1.10 g; 4.39 mmol) in CHCl3 (13 ml) maintained in the temperature range 23°-26° C. The stirring was continued for 15 minutes at 20° C. The reaction mixture was poured into a well-stirred mixture of ice (6 g) and concentrated NH4OH (1.5 ml). The two-phase system was kept at 0° for 30 minutes with continuous stirring. The system was separated and the organic phase was dried and evaporated. The desired oily product was precipitated as a hydrochloride salt and was recrystallized from CHCl3 /ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04876284 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-8526908e913b40fc90021ed6786eaae5 |
| Source note | uspto-grants-1989_10 |