HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298195Generated: November 1, 2026
N-methyl-2-pyrrolidone → Ethyl 2-(3-cyanophenyl)acetate
https://huagongshe.com/reaction/2298195
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Ethyl 3-(bromophenyl)acetate | HCID 11470552 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Water ammonium hydroxide | HCID 86589665 | — |
| Product | Ethyl 2-(3-cyanophenyl)acetate | HCID 11194802 | — |
Reaction Steps
To a mixture of of (3-bromo-phenyl)-acetic Acid ethyl ester (15.3 g, 62.9 mmol) and 1-methyl-2-pyrrolidinone (125 mL) was added copper (I) cyanide (8.46 g, 94.4 mmol). The reaction mixture was stirred in an oil bath at 190° C. for 1 h. The reaction was cooled to room temperature and was diluted with EtOAc and 2:1 H2O/NH4OH. The mixture was stirred for 10 minutes and was filtered through Celite. The aqueous layer was washed with EtOAc (2×). The organic solution was washed with 2:1 H2O/NH4OH until the aqueous extracts were no longer blue. The organic solution was dried over MgSO4, filtered and concentrated to afford (3-cyano-phenyl)-acetic Acid ethyl ester (11.95 g). 1H NMR (400 MHz, CDCl3) δ 7.51-7.58 (m, 3H), 7.43 (t, 1H), 4.16 (q, 2H), 3.63 (s, 2H), 1.25 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06492412B2 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-cdbe8809f8194f5593cdb4b3d14bf533 |
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| Source note | uspto-grants-2002_12 |
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