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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245037Generated: October 27, 2026

Cyclobutanone → 4-(4-(1-Cyanocyclobutylamino)phenyl)butanoic acid

https://huagongshe.com/reaction/245037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclobutanoneHCID 14496—
Reactant4-(4-Aminophenyl)butanoic acidHCID 27049—
ReactantTrimethylsilyl cyanideHCID 82115—
SolventEthyl AcetateHCID 8857—
Product4-(4-(1-Cyanocyclobutylamino)phenyl)butanoic acidHCID 6672204974%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-(4-aminophenyl)butyric acid (0.20 g, 1.12 mmol), cyclobutanone (0.17 mL, 2.23 mmol) and TMSCN (0.30 mL, 2.23 mmol) was heated to 80° C. and stirred for 13 h. To the medium was added ethyl acetate (2×30 mL) and then washed with water (2×30 mL). The organic layer was dried over MgSO4 and concentrated and the residue was purified with silica gel column chromatography (dichloromethane:acetone, 9:1) to give 4-[4-(1-Cyanocyclobutylamino)phenyl]butanoic acid (Formula 50) (0.21 g, 74%) as a yellowish solid. 1H NMR δ 7.06 (d, 2H, J=8.6 Hz), 6.59 (d, 2H, J=8.6 Hz), 2.75-2.83 (m, 2H), 2.59 (t, 2H, J=7.5 Hz), 2.37 (t, 2H, J=7.5 Hz), 2.33-2.42 (m, 2H), 2.11-2.28 (m, 2H), 1.92 (p, 2H, J=7.5 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658681B2
Source datasetuspto-grants-2014_02
ORD IDord-b7ff8271610c448a9635aadccacd322a
Source noteuspto-grants-2014_02