Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | HCID 86673337 | HCID 86673337 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 10331271 | HCID 10331271 | — |
Reaction Steps
To a solution of toluene-4-sulfonic acid 2-fluoro-5-nitro-benzyl ester (0.696 g, 2.13 mmoles) in 1,4-dioxane (4 mL) was added TEA (0.45 mL, 3.20 mmoles) and diethylamine (0.33 mL, 3.21 mmoles). The reaction mixture was stirred for 8 h at 55° C., concentrated and purified by TLC (petroleum ether/AcOEt/NH4OH//8/2/0.2). The expected compound was obtained as a yellow oil (0.365 g, 76% yield). MALDI-TOF: m/z 227.1 [M+H]+. 1H NMR (300 MHz, CDCl3) δ8.44; (dd, J=6.3 Hz and 2.9 Hz, 1H), 8.12; (ddd, 4-CH, J=8.9 Hz, 2.9 Hz and 4.4 Hz, 1H), 7.15; (dd, J=8.9 Hz and 8.9 Hz, 1H), 3.67; (s, 2H), 2.58; (q, J=7.1 Hz, 4H), 1.08; (t, J=7.1 Hz, 6H). 13C NMR (75 MHz, CDCl3) δ126.7; (CH, d, J=6.9 Hz), 124.1; (CH, d, J=10.2 Hz), 115.9; (CH, d, J=24.6 Hz), 49.6; (CH2), 47.1; (CH2), 11.8; (CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680095B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-d3ca1fec981e41898c31e6e9185b3140 |
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| Source note | uspto-grants-2014_03 |
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