HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 4-But-2-ynyloxy-benzenesulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 54210684 | HCID 54210684 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-But-2-ynyloxy-benzenesulfonyl chloride | HCID 11195928 | 53% |
Reaction Steps
To a solution of 0.146 g (1.0 mmol) of the product of Example 87 in 0.3 mL of dichloromethane in an acetone/ice bath under N2 was dropwise added a solution of 0.073 mL (1.1 mmol) of chlorosulfonic acid in 0.3 mL of dichloromethane. After the addition was complete, the ice bath was removed and the reaction was stirred at room temperature for 2 h. To the reaction was then dropwise added 0.113 mL (1.3 mmol) of oxalyl chloride, followed by 0.015 mL DMF. The reaction was heated to reflux for 2 h and then diluted with hexane and poured into ice water. The organic layer was washed with brine, dried over sodium sulfate, and concentrated in vacuo to provide 0.130 mg (53%) of the desired product as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06762178B2 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-2e3954a3f12340b880af19d4b4e07e6c |
| Source note | uspto-grants-2004_07 |