HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358644Generated: October 29, 2026
Dimethylformamide → Ethyl 3,3-dimethyl-5-[(phenylsulfonyl)amino]pentanoate
https://huagongshe.com/reaction/358644
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzenesulfonamide | HCID 7370 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 14536796 | HCID 14536796 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 3,3-dimethyl-5-[(phenylsulfonyl)amino]pentanoate | HCID 20066952 | — |
Reaction Steps
Benzenesulphonamide (9.6 g, 61.1 mmol) was added to a stirred solution of sodium methoxide (1.6 g, 29.6 mmol) in methanol (100 ml). The clear solution was evaporated to dryness, then dimethyl formamide (100 ml) and ethyl 5-bromo-3,3-dimethyl-pentanoate (7.0 g, 32.8 mmol) were added and the mixture was heated for eight hours at 70° C. The solution was then poured into water (600 ml), the mixture was extracted with ether and the ether phase, after being dried over sodium sulphate, was evaporated. Treatment of the solid residue with a mixture of toluene and cyclohexane (9:1) left most of the unreacted benzenesulphonamide undissolved. After filtration, the solution was evaporated and the residue was purified by chromatography on silica gel with a mixture of methylene chloride and ethanol (98:2). Yield: 4.6 g (50% of theory), oily substance, nD20 =1.5083.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04997847 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-de89c71efb1840d2ad5f68b8e41a8566 |
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| Source note | uspto-grants-1991_03 |
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