HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 86746895, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Hydroxy-N-methylbenzamide | HCID 371715 | — |
| Reactant | Ethenesulfonyl chloride | HCID 533445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86746895 | HCID 86746895 | 76.6% |
Reaction Steps
130 ml of tetrahydrofuran was added to a mixture of 7.6 g of N-benzoyl-N-methylhydroxylamine and 6.3 g of vinylsulfonyl chloride and a solution of 5.1 g of triethylamine in 20 ml of tetrahydrofuran was dropwise added to the mixture over 2 hours with stirring while cooling the mixture so that the temperature was maintained at 25° C. or less. The reaction was continued for additional 2 hours at a temperature ranging from 15° to 25° C. and then the same procedures used in Preparation Example 4 were repeated to give 9.2 g of o-vinylsulfonyl-N-benzoyl-N-methylhydroxylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05276124 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-9860880b231842728fa186ae72cdf372 |
| Source note | uspto-grants-1994_01 |