Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Dibenzo-18-crown-6 | HCID 26541 | — |
| Reactant | 2-Bromobenzocycloheptan-1-one | HCID 21703315 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Cyanobenzocycloheptan-1-one | HCID 21703316 | — |
Reaction Steps
2-cyanobenzocycloheptan-1-one (compound Ia) was prepared by dissolving 2-bromobenzocycloheptan-1-one (30.2 g, 0.126 mol) in toluene (150 mL) in a 500 mL round bottom flask equipped with a condenser. NaCN (18.6g, 0.38 mol), water (50 g), and dibenzo-18-crown-6 (0.5 g) were added to the flask. The reaction mixture was stirred vigorously at 90° C. under a static blanket of nitrogen for 15 hours. The reaction mixture was cooled and washed three times with water (70 mL×2+100 mL). The toluene solution was dried over sodium sulfate and filtered. The solvent was evaporated under reduced pressure. The residue was distilled under vacuum to give a yellow liquid (21.1 g, b.p. 158-162° C. at 17 mm Hg). The purity of the liquid was 96% by GC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06287749B1 |
|---|
| Source dataset | uspto-grants-2001_09 |
|---|
| ORD ID | ord-6a2974bbb3c64a7fb1e377db2e187bfe |
|---|
| Source note | uspto-grants-2001_09 |
|---|