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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602706Generated: October 29, 2026

Diisopropylethylamine → HCID 11374665, compound

https://huagongshe.com/reaction/602706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-[Bromo(4-chlorophenyl)methyl]benzonitrileHCID 67055351—
Reactant3-[1-(3,5-Difluorophenyl)-2,2-dimethylpropylidene]azetidineHCID 67065893—
SolventAcetonitrileHCID 6342—
ProductHCID 11374665HCID 11374665—

Reaction Steps

A mixture of 99 mg (0.32 mmol) of 3-[bromo(4-chlorophenyl)methyl]benzonitrile, 80 mg (0.216 mmol) of 3-[1-(3,5-difluorophenyl)-2,2-dimethylpropylidene]azetidine and 113 uL (0.65 mmol) of N,N-diisopropylethylamine in 3 mL of acetonitrile was heated at reflux for 3 h. Then the reaction was concentrated and the residue was dissolved in 5 ml of hexane/ether. A solution of 1 mL of 1N HCl in ether was added to above solution to make the salt. The mixture was filtered and the solids were washed with hexane/ether. The residue was neutralized with NaOH and the free base was purified by silica gel chromatography with hexanes/ethyl acetate to afford the title compound as a white solid; 1H-NMR (CDCl3) δ 1.07 (s, 9H), 3.37 (m, 2H), 4.06 (m, 2H), 4.50 (s, 1H), 6.58 (d, J=8 Hz, 2H), 6.74 (m, 1H), 7.28 (d, J=8.5 Hz, 2H), 7.34 (d, J=8.5 Hz, 2H), 7.39 (t, J=7.7 Hz, 1H), 7.50 (d, J=7.8 Hz, 1H), 7.62 (d, J=7.8 Hz, 1H), 7.72 (s, 1H); Mass Spectrum: m/e=463 (M+1 35Cl) and 465 (M+1 37Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906503B2
Source datasetuspto-grants-2011_03
ORD IDord-3a02f30aef6949e1a277dc43406939a9
Source noteuspto-grants-2011_03