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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzenesulfonamideHCID 7370—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 14536796HCID 14536796—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductEthyl 3,3-dimethyl-5-[(phenylsulfonyl)amino]pentanoateHCID 20066952—

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04997847
Source datasetuspto-grants-1991_03
ORD IDord-de89c71efb1840d2ad5f68b8e41a8566
Source noteuspto-grants-1991_03