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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19768Generated: October 26, 2026

Dimethylformamide → 4-(1-Fluorocyclobutyl)benzaldehyde

https://huagongshe.com/reaction/19768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHexaneHCID 8058—
Reactant4-CyclopropylbenzaldehydeHCID 11506474—
Reactant1-Bromo-4-(1-fluorocyclobutyl)benzeneHCID 68564159—
ReactantButyllithiumHCID 178418339—
Product4-(1-Fluorocyclobutyl)benzaldehydeHCID 84718020—

Reaction Steps

The title compound was synthesized in analogy to 4-cyclopropyl benzaldehyde (described in example S1-A) using 1.64 g of 1-bromo-4-(1-fluoro-cyclobutyl)-benzene (7.16 mmol), 4.92 ml of a 1.6 molar solution of n-BuLi in hexane (7.87 mmol) and 1.1 ml of DMF (14.32 mmol). 4-(1-Fluoro-cyclobutyl)-benzaldehyde was isolated as crude product as a light yellow liquid (1.23 g, 96%). 1H NMR (CDCl3, 300 MHz): δ 1.84 (m, 1H), 2.15 (m, 1H), 2.49-2.81 (m, 5H), 7.63 (d, J=8 Hz, 2H), 7.92 (d, J=8 Hz, 2H), 10.03 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745477B2
Source datasetuspto-grants-2010_06
ORD IDord-bb6f4adb33084144b99c3ec8cb6c4e5d
Source noteuspto-grants-2010_06