HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Cyanide → 3-hydroxy-3-cyano-3,4-dihydro-2H-1,5-benzodioxepin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Cyanide | HCID 768 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2H-1,5-Benzodioxepin-3(4H)-one | HCID 11309700 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-hydroxy-3-cyano-3,4-dihydro-2H-1,5-benzodioxepin | HCID 15557293 | — |
Reaction Steps
To a stirred solution of 4.92 g. (30 millimoles) of 3-oxo-3,4-dihydro-2H-1,5-benzodioxepin in 100 mls. of benzene is added dropwise a solution of 30 millimoles of anhydrous hydrogen cyanide in 50 ml. of benzene. The reaction mixture is stirred overnight at ambient temperature, basified with 10% sodium carbonate solution and the organic layer separated. The benzene solution is washed once with water and dried successively over anhydrous magnesium sulfate and calcium sulfate. Evaporation of the solvent under reduced pressure at 40° C. yields the crude cyanohydrin which upon purification and mixed melting point determination gives no depression with an authentic sample of 3-hydroxy-3-cyano-3,4-dihydro-2H-1,5-benzodioxepin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03944560 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-e6799d215004407bbdec444fa4284f11 |
| Source note | uspto-grants-1976_03 |