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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280471Generated: October 29, 2026

Butyl isocyanate → N-(butylaminocarbonyl)-2,3-dihydro-2,2-dimethyl-7-benzofuransulfonamide

https://huagongshe.com/reaction/280471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl isocyanateHCID 8110—
ReactantPotassium CarbonateHCID 11430—
Reactant2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-sulfonamideHCID 13424180—
SolventMethyl Ethyl KetoneHCID 6569—
ProductN-(butylaminocarbonyl)-2,3-dihydro-2,2-dimethyl-7-benzofuransulfonamideHCID 1342418184.3%

Reaction Steps

A solution of 19 g of 2,3-dihydro-2,2-dimethyl-7-benzofuransulfonamide prepared in Example 2 and 9.9 g of n-butyl isocyanate in 200 ml of 2-butanone was refluxed with 11.5 g of anhydrous potassium carbonate for 7 hours. The resulting mixture was concentrated to dryness in vacuo. The residue was taken up in 400 ml of water and extracted once with 100 ml of ethyl ether. The aqueous layer was acidified with 2N HCl and the resulting mixture was filtered and suction dried. The still slightly wet solid was washed once with 100 ml of hot acetonitrile, then suction dried an additional 8 hours to give 23 g of N-(butylaminocarbonyl)-2,3-dihydro-2,2-dimethyl-7-benzofuransulfonamide, m.p. 200°-203° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04589909
Source datasetuspto-grants-1986_05
ORD IDord-c31eca0044504bbfb9761f9214d3ea51
Source noteuspto-grants-1986_05