HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → alpha-(4-Hydroxybenzenesulfonyloxyimino)benzyl cyanide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(Hydroxyimino)-2-phenylacetonitrile | HCID 69998 | — |
| Reactant | alpha-(4-Hydroxybenzenesulfonyloxyimino)thien-2-ylacetonitrile | HCID 54023906 | — |
| Reactant | alpha-(4-Acetoxybenzenesulfonyloxyimino)benzyl cyanide | HCID 54392200 | — |
| Product | alpha-(4-Hydroxybenzenesulfonyloxyimino)benzyl cyanide | HCID 54313704 | — |
Reaction Steps
14.6 g (0.1 mole) of α-hydroxyiminobenzyl cynide (1c) are reacted with 23.46 g (0.1 mole) of 4-acetoxybenzenesulfonyl chloride (3a) in accordance with a procedure analogous to that of Example 3c. The resultant α-(4-acetoxybenzenesulfonyloxyimino)benzyl cyanide melts at 142°-143° C. 6 g of this compound are hydrolysed with a solution of NaOH in accordance with a procedure analogous to that of Example 3d, affording the title compound which, after recrystalisation from toluene, melts at 148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04736055 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-d4e33870488b4c2ca35fa36f755328bd |
| Source note | uspto-grants-1988_04 |