HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558131Generated: October 30, 2026
Hydrochloric Acid → HCID 57445080, compound
https://huagongshe.com/reaction/558131
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 2-Bromo-4-fluorobenzonitrile | HCID 118939 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Catalyst | HCID 178460666 | HCID 178460666 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 57445080 | HCID 57445080 | 44.4% |
Reaction Steps
Add ethylmagnesium bromide (3 N, 53.9 mL, 74.9 mmol) to a solution of 2-bromo-4-fluorobenzonitrile(15 g, 73.5 mmol) and tetraisopropoxytitanium (23 mL, 162 mmol) in ether (25 mL) at −70° C. under N2. After stirring at the temperature for 10 min, let it warm-up to RT and stir for one hour. Add boron trifluoride etherate (BF3OEt2) (16.8 mL, 147 mmol) to the solution slowly and stir for another hour. After adding 1 N HCl (200 mL) and ether (150 mL), separate the ether layer. Add 10% NaOH (150 mL) to the aqueous solution and extract it with ether. Separate the organic layer and dry over magnesium sulfate. Filter and concentrate in vacuo to give a residue. Purify the residue by column chromatography (diethylether) to give the title compound (7.5 g, 44%). MS (ES) m/z 230 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063035B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-41778117b3e64adaa1658bb1b94f0554 |
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| Source note | uspto-grants-2011_11 |
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