Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 131735849 | HCID 131735849 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 49837191 | HCID 49837191 | 86% |
Reaction Steps
A mixture of 8 (67 mg, 0.18 mmol) and HCl 3 N degassed (3 mL) was allowed to react at reflux for 1 h 30 min. After cooling, the reaction mixture was diluted with water (15 mL) and washed twice with diethyl ether (2×20 mL). The aqueous phase was concentrated in vacuo, affording 9 as a yellow solid (42 mg, 86% yield). Mp 118-122° C. (dec). 1H-NMR (400 MHz, DMSO): δ 2.5 (2H, d, J 4.9, BCH2), 4.42 (2H, s, PhCH2), 6.22 (1H, t, J 4.9, SO2NH), 7.49 (2H, d, J 8.6, H2, H6), 7.93 (2H, d, J 8.6, H3, H5), 7.94 (1H, s, COOH). 13C-NMR (100 MHz, DMSO): δ 31.3 (CB), 55.7, 129.7, 130.7, 131.4, 136.0, 167.6. EI-MS and elemental analysis were not obtainable, but exposure of 9 to an equimolar amount of pinacol in anhydrous THF afforded the corresponding pinacol boronate in quantitative yield and satisfactory elemental analysis; Anal. Calcd. for C15H22BNO6S: C, 50.72; H, 6.24; N, 3.94; S, 9.03. Found: C, 50.88; H, 6.41; N, 3.80; S, 8.77.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09371337B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-b88e8c6b841c494b9e6119892c28f02b |
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| Source note | uspto-grants-2016_06 |
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