HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 9-Bromo-1,2,3,4,10,10a-hexahydro-pyrazino[1,2-a]indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22338185 | HCID 22338185 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 9-Bromo-1,2,3,4,10,10a-hexahydro-pyrazino[1,2-a]indole | HCID 22338077 | 68.2% |
Reaction Steps
9-Bromo-1,2,3,4-tetrahydro-pyrazino[1,2-a]indole (3.5 g, 13.9 mmol) was dissolved in THF (15 mL) and trifluoroacetic acid (30 mL) and cooled to 0° C. Sodium borohydride (1 g, 27.9 mmol) was added in portions, the mixture was stirred for 90 min at room temperature and added to an ice/water mixture (150 mL). After addition of sodium hydroxide solution (28%, 35 mL) to render the mixture basic it was extracted with dichloromethane. Organic phases were pooled, washed with brine, dried with MgSO4 and the solvent was evaporated. Chromatography on silica gel (dichloromethane/methanol/ammonia 180:10:1) yielded 9-bromo-1,2,3,4,10,10a-hexahydro-pyrazino[1,2-a]indole (2.4 g, 68%) as a yellowish solid, MS: m/e=252.0 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07253281B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-bdc12adb43964d8b87d129c672335b9e |
| Source note | uspto-grants-2007_08 |