HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701806Generated: November 2, 2026
Carbon Dioxide → 2-Biphenylylsulfonylisocyanate
https://huagongshe.com/reaction/1701806
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Reactant | Sulphonyl diisocyanate | HCID 77898 | — |
| Reactant | 2-Phenylbenzene-1-sulfonamide | HCID 12371520 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-Biphenylylsulfonylisocyanate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04378991 |
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| Source dataset | uspto-grants-1983_04 |
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| ORD ID | ord-03fc921da2c44e558885bd04a47225f0 |
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| Source note | uspto-grants-1983_04 |
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