HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone Cyanohydrin → 2-(5H-dibenzo[a,d]cyclohepten-5-on-2-yl)propionitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone Cyanohydrin | HCID 6406 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 2-bromomethyl-5H-dibenzo[a,d]cyclohepten-5-one | HCID 12398819 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(5H-dibenzo[a,d]cyclohepten-5-on-2-yl)propionitrile | HCID 21403095 | — |
Reaction Steps
12.0 Gm. of sodium cyanide and 6.0 gm. of 2-bromomethyl-5H-dibenzo[a,d]cyclohepten-5-one are stirred at 100° C. for 40 minutes in 150 ml. of acetone cyanohydrin. The mixture is cooled and poured into ether. The ethereal layer is washed with water, dried and evaporated. The residue is chromatographed on 350 gm. of silica gel, eluting with hexane/ethyl acetate (3:2) to obtain 8.8 gm., 78%, of 5H-dibenzo[a,d]cyclohepten-5-on-2-yl acetonitrile which is recrystallized from ethyl acetate/hexane, m.p. 119°-121°- C. Use of 2-(α-bromoethyl)-5H-dibenzo[a,d]cyclohepten-5-one gives a similar yield of 2-(5H-dibenzo[a,d]cyclohepten-5-on-2-yl)propionitrile, m.p. 108°-109° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04054579 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-deae6cbf34f343fbb132b03f98785c4b |
| Source note | uspto-grants-1977_10 |