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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471548Generated: October 30, 2026

Acetic Acid → HCID 178510075, compound

https://huagongshe.com/reaction/1471548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen BromideHCID 260—
ReactantHCID 67441404HCID 67441404—
SolventWaterHCID 962—
ProductHCID 178510075HCID 17851007510%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 48% HBr (2 mL) and acetic acid (4 mL) was added 6-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-5-yloxy)-2-methoxynicotinonitrile (D46) (0.300 mg, 1.06 mmol). The reaction was stirred for 24 hours at 50° C. Water was added and the mixture was extracted with ethyl acetate. The organic layer was washed with water, brine, dried over anhydrous sodium sulfate, and then filtered. The solvent was removed under reduced pressure. The residue was purified by silica gel column (7:3 to 9:1 ethyl acetate/hexane). The material was further purified by reverse phase HPLC to give 2-hydroxy-6-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-5-yloxy)nicotinonitrile (0.027 g, 10% yield). ES(−) MS m/z=267 (M−H)−; 1H NMR (300 MHz, DMSO-d6) δ ppm 4.97 (s, 2 H), 6.4 (br s, 1 H), 7.15 (d, J=7.9 Hz, 1 H), 7.25 (s, 1 H), 7.77 (d, J=7.9 Hz, 1 H), 8.09 (d, J=7.9 Hz, 1 H), 9.24 (s, 1 H), 12.7 (br s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012431B2
Source datasetuspto-grants-2015_04
ORD IDord-9a82ce7a11524b9987cffbb4bdce21cb
Source noteuspto-grants-2015_04