HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → (2S)-(+)-(5-chloro-2-cyanophenoxy)-2,3-epoxypropane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (-)-Epichlorohydrin | HCID 2734062 | — |
| Reactant | 4-Chloro-2-hydroxybenzonitrile | HCID 3442789 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (2S)-(+)-(5-chloro-2-cyanophenoxy)-2,3-epoxypropane | HCID 10774787 | 35.2% |
Reaction Steps
A mixed solution of 5.0 g of 5-chloro-2-cyano-phenol and 6.0 g of R-(-)-epichlorohydrin was heated at 120° C. for 2 hours under a nitrogen stream. Toluene (50 ml), 0.1 g of benzyl triethylammonium chloride and 20 ml of a 30% sodium hydroxide were added, and the mixture was stirred at room temperature for 2 hours. The organic layer was separated and dried over magnesium sulfate. The solvent was then evaporated. Ethanol was added to the residue to crystallize it. The crystals were then recrystrallized from ethyl acetate to give 2.4 g (2S)-(+)-(5-chloro-2-cyanophenoxy)-2,3-epoxypropane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05130314 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-b591801eab71441b9a149272edd4de53 |
| Source note | uspto-grants-1992_07 |