HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride → HCID 20043757, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 15078420 | HCID 15078420 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20043757 | HCID 20043757 | — |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
The operation is done as in example 49, starting with 0.80 g of 5-(2-propenyloxy)pyrrolidin-2-one. After cooling to -10° C., a solution of 1.00 g of benzenesulphonyl chloride in 10 cm3 of anhydrous ether is added and the temperature is maintained at -10° C. 100 cm3 of ethyl acetate is added before filtering. Elution is done with a mixture of ethyl acetate and hexane (1-1) and by re-crystallizing from isopropyl ether, 0.20 g of product is obtained, m.p. 54°-56° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04829079 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-c3651c3b89474fd09deb35af71cec040 |
| Source note | uspto-grants-1989_05 |