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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
ReactantHCID 57722897HCID 57722897—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57722791HCID 57722791—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207186B2
Source datasetuspto-grants-2012_06
ORD IDord-b59596aa8c8e449ab262a3fb2d9f744b
Source noteuspto-grants-2012_06