HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696449Generated: October 29, 2026
3-Cyclopentyl-3-oxopropanenitrile → HCID 67272039, compound
https://huagongshe.com/reaction/1696449
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Cyclopentyl-3-oxopropanenitrile | HCID 13592118 | — |
| Reactant | HCID 67271852 | HCID 67271852 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 67272039 | HCID 67272039 | 34% |
Reaction Steps
To a mixture of (3-aminophenyl)acetic acid ethyl ester (15 g, 84 mmol) in conc. HCl (20 mL) was added sodium nitrite (6 g, 87 mmol) aqueous solution dropwise under ice-salt bath. The resulting mixture was stirred at 0° C. for 30 min and then added a solution of SnCl2.2H2O (38 g, 168 mmol) in conc. HCl dropwise also at such a rate that the reaction mixture never rose above 5° C. After the addition was completed, the mixture was stirred for another 2 h at room temperature. The precipitate was collected by suction and washed with ethyl ether to afford (3-Hydrazinophenyl)acetic acid ethyl ester hydrochloride (17 g, 88%) as a brown solid. MS (ESI) m/z: 195 (M+H+). A solution of (3-hydrazinophenyl)acetic acid ethyl ester hydrochloride (17 g, 74 mmol) and 3-cyclopentyl-3-oxopropionitrile (12.2 g, 88.8 mol) in alcohol (150 mL) containing conc. HCl (10 mL) was heated to reflux overnight. After removed of the solvent, the precipitate was collected by suction and washed with ethyl ether to afford the crude product, which was purified by column chromatography to afford [3-(5-amino-3-cyclopentylpyrazol-1-yl)phenyl]acetic acid ethyl ester hydrochloride (8.8 g, 34% yield) as a yellow solid. 1H NMR (300 MHz, DMSO-d6): δ 7.40-7.66 (m, 4H), 5.68 (s, 1H), 4.05 (q, J=7.2 Hz, 2H), 3.75 (s, 2H), 3.00-3.08 (m, 1H), 1.98-2.00 (m, 2H), 1.58-1.70 (m, 6H), 1.17 (t, J=7.2 Hz, 3H); MS (ESI) m/z: 314 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163756B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-80f6cb815db14219b65ba7d5d6b7a38e |
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| Source note | uspto-grants-2012_04 |
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