HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256062Generated: October 26, 2026
N-(3-Fluorophenyl)acetamide → 4-Acetamido-2-fluorobenzene-1-sulfonyl chloride
https://huagongshe.com/reaction/1256062
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-(3-Fluorophenyl)acetamide | HCID 9594 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Product | 4-Acetamido-2-fluorobenzene-1-sulfonyl chloride | HCID 16771084 | 18% |
Reaction Steps
Neat N-(3-fluorophenyl)acetamide (5 g, 32.65 mmol) was put on an ice-water bath and had chlorosulfonic acid added drop-wise. The solution was stirred at 0° C. for one hour, and was then stirred at room temperature overnight. The reaction was then stirred at 50° C. for four hours. The solution was then cooled to room temperature and added to a beaker of ice water. The ice was allowed to melt and then the solution was extracted with ethyl ether. The organic layer was washed with brine, then dried over sodium sulfate, and filtered. The solvent was removed under slightly reduced pressure to give 4-acetamido-2-fluorobenzene-1-sulfonyl chloride (1.50 g, 18% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08461134B2 |
|---|
| Source dataset | uspto-grants-2013_06 |
|---|
| ORD ID | ord-ebdf9e4656c14f49b9d40ee40e1da855 |
|---|
| Source note | uspto-grants-2013_06 |
|---|