HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561772Generated: October 26, 2026
Methanesulfonamide → 5-Bromo-N-methanesulfonylpentanamide
https://huagongshe.com/reaction/561772
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | 5-Bromovaleryl chloride | HCID 521173 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Bromo-N-methanesulfonylpentanamide | HCID 20296141 | 88.3% |
Reaction Steps
A mixture consisting of methanesulfonamide (4.76 g) and 5-bromovaleric acid chloride (10 g) was heated at 85-90° C. for one hour, was cooled to room temperature, and was diluted with ethyl acetate (75 mL). The solution was washed with water, brine, and dried over sodium sulfate. The solution was filtered and evaporated to 40 mL of solvent, then cooled to −15° C. A white precipitate formed, which was collected by filtration to afford the title intermediate (11.4 g, 88%) as a white solid; melting point 98-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063240B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-4ccd0fc749d9494d93f44d84999ebb6f |
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| Source note | uspto-grants-2011_11 |
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