HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450727Generated: October 26, 2026
Acetonitrile → 2,3-Dihydro-1H-indene-2-carbonitrile
https://huagongshe.com/reaction/450727
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 2,3-Dihydro-1h-inden-2-yl methanesulfonate | HCID 255221 | — |
| Catalyst | Tetraethylammonium cyanide | HCID 3014735 | — |
| Product | 2,3-Dihydro-1H-indene-2-carbonitrile | HCID 23239618 | 52% |
Reaction Steps
A mixture of methanesulfonic acid indan-2-yl ester (18.65 g, 87.9 mmol) and tetraethylammonium cyanide (15.10 g) in acetonitrile (180 mL) was heated to 55° C. for 5 hours, cooled and concentrated. The residue was partitioned between ethyl acetate and water, and the organic phase separated. This was dried over MgSO4 and the filtered solution was concentrated and then separated by column chromatography (dichloromethane:ethyl acetate, 6:1-1:1) to give the product as a red solid (6.51 g, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486984B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-b09be4f86e70459ba16dd2d42dc4a312 |
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| Source note | uspto-grants-2013_07 |
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