HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4,5-dihydro-8-methoxy-1H-benz[g]indol-1-yl-propan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | (S)-(+)-1-Aminopropan-2-ol | HCID 7311736 | — |
| Reactant | (RS)-2-(2-oxoethyl)-7-methoxy-1-tetralone | HCID 19036405 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4,5-dihydro-8-methoxy-1H-benz[g]indol-1-yl-propan-2-ol | HCID 19036507 | — |
Reaction Steps
A solution of 3 g of (RS)-2-(2-oxoethyl)-7-methoxy-1-tetralone and 150 mg of p-toluenesulfonic acid in 130 ml in anhydrous toluene was heated on a water separator. A solution of 4.16 g of (S)-1-amino-2-propanol in 20 ml of anhydrous toluene was added dropwise to the boiling solution over a period of 5 minutes. Subsequently, the mixture was boiled for an additional 30 minutes, during which the solvent was reduced to a volume of 25 ml. The cooled reaction mixture was purified by column chromatography on silica gel (ethyl acetate/toluene 1:1). 3.0 g (84%) of (S)-1-(4,5-dihydro-8-methoxy-1H-benz[g]indol-1-yl-propan-2-ol were obtained as a brown oil which was used directly in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05646173 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-934f9472c9d0443f93505d820829fd92 |
| Source note | uspto-grants-1997_07 |