HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219878Generated: October 30, 2026
Potassium Carbonate → tert-butyl N-(5-cyano-2-fluorobenzyl)-N-methylglycinate
https://huagongshe.com/reaction/219878
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sarcosine t-butyl ester hydrochloride | HCID 11252350 | — |
| Reactant | 3-(Bromomethyl)-4-fluorobenzonitrile | HCID 16227236 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | tert-butyl N-(5-cyano-2-fluorobenzyl)-N-methylglycinate | HCID 67529926 | — |
Reaction Steps
A mixture of 5-cyano-2-fluorobenzylbromide (CARBOCORE; CO-0137; 1.50 g; 7.01 mmol; 1 eq.), sarcosine tert-butyl ester hydrochloride (BACHEM; F-1135; 1 527.73 mg; 8.41 mmol; 1.20 eq.) and potassium carbonate (2.91 g; 21.02 mmol; 3 eq.) in CH3CN (25 mL) was stirred at 60° C. for 6 hours then at RT for one night. The acetonitrile was evaporated in vacuo and the resulting mixture diluted with water. Extraction with EtOAc, washing with NaCl sat. solution, drying over magnesium sulfate and concentration in vacuo gave the title compound as a slightly yellow oil (1.9 g; 97%). 1H NMR (CDCl3) δ 7.86 (dd, J=6.5, 2.0 Hz, 1H), 7.59-7.53 (m, 1H), 7.13 (t, J=9.0 Hz, 1H), 3.78 (s, 2H), 3.23 (s, 2H), 2.38 (s, 3H), 1.49 (s, 9H). 19F NMR (CDCl3) δ-108.3. GC/MS: 278. LC/MS (Method B): 279.1 (M+H)+. HPLC (Method A) Rt 2.25 min (Purity: 91.4%).
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-aa8828141f2547d6805209557794760e |
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| Source note | uspto-grants-2012_06 |
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