HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trichloroacetic Acid → 3,4-Dihydro-5-methyl-1(2H)-isoquinolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trichloroacetic Acid | HCID 6421 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 4-Methyl-1-indanone | HCID 4418431 | — |
| Product | 3,4-Dihydro-5-methyl-1(2H)-isoquinolinone | HCID 148140 | 47.2% |
Reaction Steps
A mixture of 4.7 g (32.2 mmol) of 2,3-dihydro-4-methyl-1H-inden-1-one and 53 g of trichloroacetic acid was heated to 65°. To the resulting solution was added 4.2 g (64.4 mmol) of sodium azide and the mixture was kept at 65° for 18 hours. An additional 1.0 g of sodium azide was then added and heating continued for another four hours. The mixture was diluted with 200 ml of ice water and extracted with ether. The ether extracts were washed with water, saturated sodium hydrogen carbonate, dried (MgSO4), and concentrated. The residue was chromatographed (SiO2, ether to ether/methanol 95/5). The resulting product was recrystallized from toluene to give 2.45 g (47%) of product; mp 141°-143°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05177075 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-004b3a8eb7984ec59b486de9877e9986 |
| Source note | uspto-grants-1993_01 |