HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Sulfate → HCID 15615996, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Sulfate | HCID 6163 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 14517965 | HCID 14517965 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15615996 | HCID 15615996 | — |
Reaction Steps
In this example 2 g of 3-trifluoromethylbenzylsulfonamidoacetamide was dissolved in 30 ml of dichloromethane. To this was added 0.32 g of sodium hydroxide dissolved in a minimum amount of water and 0.46 of benzyltriethylammonium chloride. A solution of 1.1 ml of diethylsulfate in 5 ml of dichloromethane was added dropwise. The reaction mixture was stirred overnight at room temperature. Water was added to the reaction mixture, and the dichloromethane layer was separated. The water phase is extracted with dichloromethane. The organic phases are combined, dried over magnesium sulfate, filtered and stripped. Trituration of the resulting solid residue yielded 1.4 g of title compound as a white solid; m.p. 67° to 68.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04885027 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-4c49a9d70990429fa7a0674c15e7f948 |
| Source note | uspto-grants-1989_12 |