HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716663Generated: October 27, 2026
Chlorosulfonyl isocyanate → 4-Bromo-1H-indole-3-carbonitrile
https://huagongshe.com/reaction/1716663
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | 4-Bromoindole | HCID 676494 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Bromo-1H-indole-3-carbonitrile | HCID 2763232 | — |
Reaction Steps
To a 0° C. solution of 4-bromoindole (5 g, 25.5 mmol) in acetonitrile (50 ml) was added dropwise chlorsulfonylisocyanate (2.37 ml, 27.3 mmol) over a 5 minute period. The reaction mixture was stirred at 0° C. for 2 hours, and TEA (3.77 ml, 27.0) was added dropwise over a 10 minute period. The reaction mixture was allowed reach room temperature overnight, poured into ice/water mixture (200 ml), and the aqueous layer was extracted with EtOAc. The combined organic extracts were dried over Na2SO4, filtered, concentrated, and purified by flash chromatography to afford 4-bromo-1H-indole-3-carbonitrile LVII as an off-white solid (4.9 g, 87% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07803830B2 |
|---|
| Source dataset | uspto-grants-2010_09 |
|---|
| ORD ID | ord-f71d0473fa5b42a8b07b70b4a9f07b2d |
|---|
| Source note | uspto-grants-2010_09 |
|---|