HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338388Generated: October 30, 2026
Cyclobutanone → 2-Bromo-5-(1-hydroxycyclobutyl)benzonitrile
https://huagongshe.com/reaction/338388
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclobutanone | HCID 14496 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 2-Bromo-5-iodobenzonitrile | HCID 45040712 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-5-(1-hydroxycyclobutyl)benzonitrile | HCID 86698729 | — |
Reaction Steps
To 2-bromo-5-iodobenzonitrile (1457 mg, 4.730 mmol) in tetrahydrofuran (10 mL) at −40° C. was added isopropyl magnesium chloride.lithium chloride (1.3M in THF, 4.4 mL, 5.7 mmol) dropwise. The mixture was stirred at −40° C. for 10 minutes, and was then treated with cyclobutanone (0.4 mL, 5.2 mmol) dropwise at −40° C. The reaction mixture was warmed to room temperature and stirred at that temperature for 16 hours. The reaction mixture was poured into water (10 mL) and extracted with ethyl acetate (3×20 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to give the title compound which was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889730B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-0775dc3269994b5da2b902618f009bc0 |
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| Source note | uspto-grants-2014_11 |
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