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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761901Generated: October 30, 2026

Hydrochloric Acid → Hepsulfam

https://huagongshe.com/reaction/1761901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,7-HeptanediolHCID 12381—
ReactantChlorosulfamic acidHCID 24499—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHepsulfamHCID 10060663.1%

Reaction Steps

A 57% oil dispersion of sodium hydride (11.8 g, 0.28 mole NaH) was added to 150 ml of tetrahydrofuran. The suspension was stirred and gently heated, and 15.84 g (0.12 mole) of 1,7-heptanediol in 75 ml of tetrahydrofuran was added gradually over a period of 90 minutes. An additional 25 ml of tetrahydrofuran was then added, and the reaction mixture was stirred at reflux for five hours. An additional 150 ml of tetrahydrofuran was added, and to the stirred warm mixture there was added dropwise a solution of 28.9 g (0.25 mole) of sulfamoyl chloride in 150 ml of tetrahydrofuran over a two hour period. The reaction mixture was stirred at reflux for five hours, then cooled and treaated dropwise with 125 ml of water. The mixture was acidified with 2N hydrochloric acid, and the organic layer was separated and dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue triturated with ethyl acetate to give a yellow solid which was recrystallized from an ethyl acetate--hexane mixture to give 22.0 g of 1,7-heptanediol disulfamate as colorless granules, m.p. 87°-88° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04829084
Source datasetuspto-grants-1989_05
ORD IDord-79e471cba6984de885a9657bf1eb3d6d
Source noteuspto-grants-1989_05