HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl bromide → HCID 131715243, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 103603-13-0 | HCID 13603301 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 131715243 | HCID 131715243 | — |
Reaction Steps
A solution of dl-8-amino-4,4a,5,6-tetrahydro-2H-benzo(h)-cinnolin-3-one (3 g) and n-butyl-bromide (5.7 g) in acetone (75 ml) is heated at reflux temperature in the presence of fine powdered potassium carbonate (5 g). The mixture is filtered, the acetone is evaporated and the residue is partitioned between water and ethyl acetate. The usual work-up affords a crude compound (3.9 g) which is crystallized from methanol to yield dl-1-n-butyl-8-amino-4,4a,5,6-tetrahydro-2H-benzo(h)-cinnolin-3-one m.p. 141°-142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04692447 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-8a4797082807483782e1455feeb51dfb |
| Source note | uspto-grants-1987_09 |