HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839690Generated: October 30, 2026
Potassium Iodide → (1-Oxo-2-methyl-2-phenyl-6,7-dichloro-5-indanyloxy)acetonitrile
https://huagongshe.com/reaction/839690
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6,7-Dichloro-5-hydroxy-2-methyl-2-phenylindan-1-one | HCID 93690 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (1-Oxo-2-methyl-2-phenyl-6,7-dichloro-5-indanyloxy)acetonitrile | HCID 12423629 | — |
Reaction Steps
2-Methyl-2-phenyl-5-hydroxy-6,7-dichloro-1-indanone (4.61 g., 0.015 mole), chloroacetonitrile (1.13 g., 0.015 mole), potassium carbonate (2.08 g., 0.015 mole), potassium iodide (0.25 g., 0.0015 mole) and acetone (75 ml.) are heated at reflux for 23 hours. The reaction mixture is cooled to 25° C. and concentrated to dryness in vacuo to give an oily residue which on trituration with water gives 5.12 g. of (1-oxo-2-methyl-2-phenyl-6,7-dichloro-5-indanyloxy)acetonitrile which melts at 163°-165° C. on crystallization from cyclohexane:benzene, 5:1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04096267 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-fbbf1dda4de7448281654b6a1cf10a25 |
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| Source note | uspto-grants-1978_06 |
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