HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222300Generated: October 30, 2026
9-Borabicyclo(3.3.1)nonane → HCID 57722791, compound
https://huagongshe.com/reaction/222300
Participants
| Role | Name | HCID | Charge |
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| Reactant | 9-Borabicyclo(3.3.1)nonane | HCID 78966 | — |
| Reactant | HCID 57722897 | HCID 57722897 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57722791 | HCID 57722791 | — |
Reaction Steps
3-chloro-7-vinyl-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-5-one (20 mg, 0.075 mmol) was dissolved in 1 mL of tetrahydrofuran. RH(COD)2BF4 (3 mg, 0.007 mmol) was added followed by a dropwise addition of 9-BBN (0.44 mL of 0.5 M in THF, 0.22 mmol) and the reaction was stirred overnight. The reaction was cooled to 0° C. and quenched by the simultaneous addition of 1M sodium hydroxide (2.5 ml) and 30% aqueous hydrogen peroxide (0.75 mL) and stirred for 5 hours. The resulting solution was poured into ethyl acetate and brine and extracted three times with ethyl acetate. The combined organics were dried over magnesium sulfate, dried over magnesium sulfate, concentrated in vacuo, and purified via flash chromatography (0-60% ethyl acetate/hexanes) to afford the title compound. 1H NMR (600 MHz, CDCl3) δ 8.41 (s, 1H); 8.03 (s, 1H); 7.54 (s, 1H); 7.28 (m, 2H); 7.17-7.14 (m, 2H); 5.31 (s, 1H); 2.70 (q, 2H); 1.25 (t, 3H). Hydroxyl proton was not observed. LRMS (APCI) calc'd for (C16H15ClNO) [M+H]+, 272.1; found 272.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207186B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-b59596aa8c8e449ab262a3fb2d9f744b |
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| Source note | uspto-grants-2012_06 |
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