HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458206Generated: November 2, 2026
Hydrochloric Acid → 2-Cyano-phenylboric acid
https://huagongshe.com/reaction/1458206
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 2-Bromobenzonitrile | HCID 16272 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Pentane | HCID 8003 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Cyano-phenylboric acid | HCID 21708089 | 55.7% |
Reaction Steps
12.4 ml of a 1.6M solution of t-butyllithium in n-pentane was dropwise added to 23 ml of THF at -76° C. in about 10 minutes. Then, a solution of 2.0 g (11.0 mmol) of 2-bromobenzonitrile in 3.0 ml of THF was dropwise added to the resulting mixture at -76° C. in about 20 minutes, followed by the dropwise addition of 2.3 ml (19.8 mmol) of trimethoxyborane in 7 minutes. The obtained mixture was stirred at -76° C. for 20 minutes, followed by the addition of 13.8 ml of 2N hydrochloric acid. The obtained mixture was stirred at room temperature for 30 minutes and extracted with ethyl acetate. The ethyl acetate phase was washed with water and a saturated brine, dried and distilled to remove the solvent. 15 ml of methylene chloride and 15 ml of n-hexane were added to the obtained residue. The obtained mixture was stirred at room temperature for 30 minutes to give a precipitate. The precipitate was recovered by filtration and dried to give 0.9 g of the title compound (yield: 55.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05849912 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-15bfbefa11c64c289c937f3e0973d147 |
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| Source note | uspto-grants-1998_12 |
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