Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701806Generated: November 2, 2026

Carbon Dioxide → 2-Biphenylylsulfonylisocyanate

https://huagongshe.com/reaction/1701806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantPhosgeneHCID 6371—
ReactantButyl isocyanateHCID 8110—
ReactantSulphonyl diisocyanateHCID 77898—
Reactant2-Phenylbenzene-1-sulfonamideHCID 12371520—
SolventO-XyleneHCID 7237—
Product2-BiphenylylsulfonylisocyanateHCID 13103320—

Reaction Steps

Into a dry, 500 ml, 3 neck round bottom flask, equipped with a dry-ice-cooled reflux condenser, stirrer, gas inlet tube and thermometer was charged 12 g of 1,1'-biphenyl-2-sulfonamide, 100 ml of xylene, 0.2 g of 1,4-diaza[2.2.2]bicyclooctane (DABCO) and 5 g of n-butyl isocyanate. The mixture was heated to 135° and then phosgene was passed into the system until the temperature dropped to 125°. Heating was continued to bring the mixture up to 135° and additional phosgene was added to lower the temperature to 120°. This cycling was repeated until the temperature of the refluxing mixture remained at 120° without further addition of phosgene. The mixture was then allowed to cool to room temperature, filtered and concentrated in vacuo. Any contact with moisture was scrupulously avoided due to the extreme reactivity of the sulfonyl isocyanate. The product thus obtained (yield 10.4 g) showed an absorption peak in the infrared spectrum at 2200 cm-1, consistent with a sulfonyl isocyanate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04378991
Source datasetuspto-grants-1983_04
ORD IDord-03fc921da2c44e558885bd04a47225f0
Source noteuspto-grants-1983_04