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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192799Generated: November 1, 2026

1-Chloro-4-iodobenzene → HCID 66957737, compound

https://huagongshe.com/reaction/1192799

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-iodobenzeneHCID 12510—
ReactantSodium SulfateHCID 24436—
ReactantSodium AzideHCID 33557—
ReactantL-ProlineHCID 145742—
Reactant4-EthynylbenzonitrileHCID 4547245—
ReactantL-Ascorbic AcidHCID 54670067—
CatalystCopper SulfateHCID 24462—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 66957737HCID 6695773748.9%

Reaction Conditions

Temperature65 °C

Reaction Steps

Following the procedure published by Feldman et al. (Org Lett. 2004, 6, 3897), a suspension of 4-ethynylbenzonitrile (50 mg, 0.393 mmol), 1-chloro-4-iodobenzene (94 mg, 0.393 mmol), L-proline (9 mg, 0.079 mmol), ascorbic acid (7 mg, 0.039 mmol), NaN3 (31 mg, 0.472 mmol), CuSO4 (3 mg, 0.020 mmol), and Na2SO4 (11 mg, 0.079 mmol) in DMSO (1.5 mL) was heated at 65° C. for 24 h. Upon cooling the mixture was diluted with H2O and stirred for 30 min at ambient temperature. The intermediate 4-[1-(4-chlorophenyl)-1H[1,2,3]triazol-4-yl]-benzonitrile (54 mg, 48%) was then obtained by vacuum filtration after washing with copious volumes of H2O and 20% NH4OH (˜20 mL). Reduction to the aldehyde was then conducted under conditions previously described.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680269B2
Source datasetuspto-grants-2014_03
ORD IDord-f89386a646c74c47a5ce7665ed1096e0
Source noteuspto-grants-2014_03