HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 4,4-Dimethyl-1-phenyl-1,2,3,4-tetrahydroisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4,4-Dimethyl-1-phenyl-3,4-dihydroisoquinoline | HCID 13728598 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4,4-Dimethyl-1-phenyl-1,2,3,4-tetrahydroisoquinoline | HCID 56686978 | 4% |
Reaction Steps
A solution of 471 mg (2.0 mmol) of 4,4-dimethyl-1-phenyl-3,4-dihydroisoquinoline in MeOH (6 ml) was cooled to 0° C. and 151 mg (4.0 mmol) of NaBH4 were added in portions. After stirring for 3 h at RT a saturated aqueous NH4Cl solution was added. Then most of the methanol was removed under vacuum and the residue was extracted with EE. The organic phase was washed with brine, dried over Na2SO4, filtered and concentrated to small volume under vacuum. 19 mg (0.08 mmol, 4%) of 4,4-dimethyl-1-phenyl-1,2,3,4-tetrahydroisoquinoline were obtained as the residue, which was reacted further with no additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367700B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-72e706a3014a4eb3aa429a5b55574ef3 |
| Source note | uspto-grants-2013_02 |