HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730116Generated: November 1, 2026
Hydrochloric Acid → Ethyl 7-(methanesulfonamido)heptanoate
https://huagongshe.com/reaction/1730116
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | Ethyl 7-bromoheptanoate | HCID 122490 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 7-(methanesulfonamido)heptanoate | HCID 12150839 | — |
Reaction Steps
A stirred suspension of sodium hydride (57% in mineral oil) (2.33 g., 0.055 mole) in a solvent mixture of benzene (50 ml.) and dimethylformamide (50 ml.) is treated, over 30 minutes, with methanesulfonamide (4.75 g., 0.055 mole). This mixture is heated on the steam bath for 1.5 hours, then cooled to room temperature. At this temperature is added ethyl 7-bromoheptanoate (13 g., 0.055 mole) and the reaction mixture is heated at 90° C. for 20 hours. The reaction is poured into ater (200 ml.), neutralized with hydrochloric acid and extracted with ethyl acetate (2 × 100 ml.). The ethyl acetate layer is washed with brine, dried over sodium sulfate, then concentrated in vacuo. The yield of ethyl 7-(methanesulfonamido)heptanoate is 7.1 g. (51%) boiling 165°-168°/0.1 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03991106 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-4c229f87bfee4431976ce88fb0c42623 |
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| Source note | uspto-grants-1976_11 |
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