HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384860Generated: October 31, 2026
Benzenesulfonyl chloride → HCID 18449980, compound
https://huagongshe.com/reaction/384860
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | HCID 18450056 | HCID 18450056 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18449980 | HCID 18449980 | — |
Reaction Steps
To a cooled (−78° C.) solution of propionic acid (27) (96.3 mg, 0.510 mmol) in tetrahydrofuran (10 ml), n-butyl lithium (1.40 ml, 2.24 mol) was added next and stirred for 30 minutes at −78° C. Benzene sulfonyl chloride (277 mg, 1.5 mmol) was added next, and the reaction was stirred for 16-24 hours, allowing temperature to rise from −78° C. to ambient conditions. The reaction was then diluted with ethyl acetate, and 1M HCl was added to adjust the pH to 1-2. The layers were then separated, and the organic layer was placed over magnesium sulfate and concentrated under reduced pressure. The crude material was then purified by flash chromatography with silica, eluting with 5% methanol in dichloromethane to yield the desire product (22) as a white solid. (M−1=386.4)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08367828B2 |
|---|
| Source dataset | uspto-grants-2013_02 |
|---|
| ORD ID | ord-51f0d4a1dfd345a1bf1062bde9236169 |
|---|
| Source note | uspto-grants-2013_02 |
|---|