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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118423Generated: November 2, 2026

Butyl isocyanate → HCID 13937615, compound

https://huagongshe.com/reaction/2118423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl isocyanateHCID 8110—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 13937614HCID 13937614—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 13937615HCID 13937615—

Reaction Steps

A mixture of 7.7 g of the product from Example 4, 3.5 g of n-butyl isocyanate, and 4.8 g anhydrous potassium carbonate in 100 ml of methyl ethyl ketone was stirred at reflux temperature for 4 hours. After cooling to room temperature, the reaction mixture was concentrated to approximately one-third volume and diluted with 150 ml of water. The resulting solid was collected by filtration and washed with one portion of water and one portion of n-butyl chloride. The yield of N-[(n-butyl)aminocarbonyl]-2-(methoxycarbonyl)-6-nitrophenylmethanesulfonamide, m.p. 144°-150°, was 9.1 g as a tan solid; IR(nujol): 1725, 1665 cm-1, NMR (CDCl3 /DMSO-d6): δ 0.6-1.7 (7H, m), 2.9-3.4 (2H, m), 4.0 (3H, s, CO2CH3), 5.7 (2H, s, --CH2 --), 7.4-8.3 (3H, m), 10.5 (1H, br s, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04678500
Source datasetuspto-grants-1987_07
ORD IDord-896241b0e47645f4adde7c9a6b922863
Source noteuspto-grants-1987_07