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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclobutanoneHCID 14496—
ReactantLithium ChlorideHCID 433294—
Reactant2-Bromo-5-iodobenzonitrileHCID 45040712—
ReactantHCID 178418918HCID 178418918—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-5-(1-hydroxycyclobutyl)benzonitrileHCID 86698729—

Reaction Conditions

Temperature-40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-0775dc3269994b5da2b902618f009bc0
Source noteuspto-grants-2014_11