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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372512Generated: October 31, 2026

Hydrochloric Acid → Ethyl 7-(methanesulfonamido)heptanoate

https://huagongshe.com/reaction/372512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantMethanesulfonamideHCID 72879—
ReactantEthyl 7-bromoheptanoateHCID 122490—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl 7-(methanesulfonamido)heptanoateHCID 12150839—

Reaction Steps

A stirred suspension of sodium hydride (57%) (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 is heated at 90° C. for twenty hours. The reaction is poured into water (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 numberUS04091107
Source datasetuspto-grants-1978_05
ORD IDord-39f0852869424d448435c9aca4d1bb30
Source noteuspto-grants-1978_05