Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Bromoacetamide | HCID 69632 | — |
| Reactant | Ethyl 2-(1,6-dihydroxy-4-methyl-1,3-dihydrobenzo[c][1,2]oxaborol-3-yl)acetate | HCID 58292549 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58292874 | HCID 58292874 | — |
Reaction Steps
To a solution of (1,6-dihydroxy-4-methyl-1,3-dihydro-benzo[c][1,2]oxaborol-3-yl)-acetic acid ethyl ester (0.2 g, 0.8 mmol) in anhydrous DMF (3 mL) was added sodium hydride (0.08 g, 2.0 mmol). After stirring for 15 minutes 2-bromo-acetamide (0.166 g, 1.2 mmol) was added and the resulting mixture stirred at room temperature for 18 hours then quenched with crushed ice. The pH was adjusted to 3 with 6M HCl and the mixture extracted with EtOAc. The organic extracts were washed with water, brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by silica gel flash column chromatography (0-5% MeOH in DCM) to give 6-carbamoylmethoxy-1-hydroxy-4-methyl-1,3-dihydro-benzo[c][1,2]oxaborol-3-yl)-acetic acid ethyl ester (0.13 g, 53%). 1H NMR 400 MHz (DMSO-d6) δ 9.17 (s, 1H), 7.47 (s, 1H), 7.36 (s, 1H), 7.02 (s, 1H), 6.89 (s, 1H), 5.45 (m, 1H), 4.40 (s, 2H), 4.09-4.02 (m, 2H), 3.10 (dd, J=15.2, 2.4 Hz, 1H), 2.26-2.17 (m, 4H), 1.17-1.04 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08343944B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-9753c4e1a0ee423fbcaa0081e5fe2faf |
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| Source note | uspto-grants-2013_01 |
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