Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054731Generated: November 2, 2026

Cyclobutanone → 2-Bromo-5-(1-hydroxycyclobutyl)benzonitrile

https://huagongshe.com/reaction/1054731

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 (1.3 M 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 numberUS09394285B2
Source datasetuspto-grants-2016_07
ORD IDord-1cd63c9f4e3d4b2abfdef4b0df56f9ff
Source noteuspto-grants-2016_07