HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219885Generated: October 26, 2026
Potassium Carbonate → tert-butyl N-(5-cyano-2-fluorobenzyl)-N-methyl-beta-alaninate
https://huagongshe.com/reaction/219885
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tert-butyl 3-(methylamino)propanoate | HCID 14760311 | — |
| Reactant | 3-(Bromomethyl)-4-fluorobenzonitrile | HCID 16227236 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | tert-butyl N-(5-cyano-2-fluorobenzyl)-N-methyl-beta-alaninate | HCID 66677998 | — |
Reaction Steps
A mixture of 5-cyano-2-fluorobenzylbromide (CARBOCORE; CO-0137; 1.50 g; 7.01 mmol; 1 eq.), tert-butyl N-methyl-beta-alaninate (1.34 g; 8.41 mmol; 1.20 eq.) (prepared as described by Howard N., I. et al. in Bioorg. Med. Chem. 11 (2003), 3083-3099) and potassium carbonate (1.94 g; 14.02 mmol; 2 eq.) in CH3CN (25 mL) was stirred at 60° C. for 6 hours then at RT for 16 hours. The acetonitrile was evaporated in vacuo and the resulting mixture diluted with water. Extraction with EtOAc, washing with NaCl sat. solution, drying over sodium sulfate and concentration in vacuo gave title compound as a slightly yellow oil (1.9 g; 92%). 1H NMR (CDCl3) δ 7.79 (dd, J=6.7, 2.1 Hz, 1H), 7.57-7.52 (m, 1H), 7.11 (t, J=8.9 Hz, 1H), 3.57 (s, 2H), 2.74 (t, J=7.1 Hz, 2H), 2.43 (t, J=7.1 Hz, 2H), 2.22 (s, 3H), 1.45 (s, 9H). LC/MS (Method B): 293.2 (M+H)+. HPLC (Method A) Rt 2.44 min (Purity: 86.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202865B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-c8ca3a328c884567a1cdf62584df45a8 |
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| Source note | uspto-grants-2012_06 |
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