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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730116Generated: November 1, 2026

Hydrochloric Acid → Ethyl 7-(methanesulfonamido)heptanoate

https://huagongshe.com/reaction/1730116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantMethanesulfonamideHCID 72879—
ReactantEthyl 7-bromoheptanoateHCID 122490—
SolventBenzeneHCID 241—
SolventDimethylformamideHCID 6228—
ProductEthyl 7-(methanesulfonamido)heptanoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03991106
Source datasetuspto-grants-1976_11
ORD IDord-4c229f87bfee4431976ce88fb0c42623
Source noteuspto-grants-1976_11