HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283378Generated: November 1, 2026
Chlorosulfonyl isocyanate → HCID 86632011, compound
https://huagongshe.com/reaction/2283378
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | Indan-5-amine | HCID 90496 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Nitroethane | HCID 6587 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86632011 | HCID 86632011 | 41.7% |
Reaction Steps
Sulfurisocyanatidic chloride (0.752 mL, 8.63 mmol) and anhydrous nitroethane (10 mL) were mixed, cooled to −5° C. (ice/salt-bath) and a solution of 2,3-dihydro-1H-inden-5-amine (1 g, 7.51 mmol) in anhydrous nitroethane (10 mL) was added dropwise under vigorous stirring. When the addition was completed, anhydrous aluminum chloride (1.251 g, 9.39 mmol) was added and the suspension was heated at 110° C. for 60 min. The solution was cooled to room temperature and diluted with water (50 mL) and ethyl acetate (50 mL). The mixture was filtered and the layers were separated. The organic phase was dried over magnesium sulfate and concentrated under vacuum. The residue was dissolved in sulfuric acid and water (1:1 30 mL) and heated at 140° C. for 90 min before it was allowed to reach room temperature and stirred over night. The mixture was neutralized using 15% sodium hydroxide and extracted with ethyl acetate. The combined organic phases were dried over magnesium sulfate and concentrated under vacuum to give 0.664 g (21% yield) of the title mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145380B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-a83a392067b9495bb40f5148cc6a12bc |
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| Source note | uspto-grants-2015_09 |
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