HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404308Generated: October 31, 2026
Potassium Carbonate → tert-butyl N-(4-cyano-2-fluorobenzyl)-N-methylglycinate
https://huagongshe.com/reaction/2404308
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Bromomethyl)-3-fluorobenzonitrile | HCID 2783149 | — |
| Reactant | Sarcosine t-butyl ester hydrochloride | HCID 11252350 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | tert-butyl N-(4-cyano-2-fluorobenzyl)-N-methylglycinate | HCID 66677678 | 99.8% |
Reaction Steps
A mixture of 4-cyano-2-fluorobenzyl bromide (250 g, 1.17 mol), sarcosine tert-butyl ester hydrochloride (212.2 g, 1.17 mol) and potassium carbonate (484 g, 3.50 mol) in acetone (2 L) was stirred 24 hours at 50° C. and 18 hours at RT. The reaction mixture was filtered and the filtrate was concentrated under vacuum. The residue was taken up with water (1 L) and extracted with ethyl acetate (2×1 L). The combined organic layers were washed with water (1 L), dried (MgSO4) and concentrated under vacuum to give the title compound as a yellow-brown oil (325 g, quantitative). 1H NMR (DMSO-d6, 300 MHz) δ 7.82 (dd, J=9.9, 1.4 Hz, 1H), 7.70 (dd, J=7.9, 1.5 Hz, 1H), 7.64 (m, 1H), 3.78 (s, 2H), 3.23 (s, 2H), 2.27 (s, 3H), 1.42 (s, 9H). LC/MS (Method B): 279.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802704B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-9da44555de3143b2883cd780d65e232c |
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| Source note | uspto-grants-2014_08 |
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