Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485057Generated: October 31, 2026

4-Hydroxybenzaldehyde → 4-(Cyclobutylmethoxy)benzaldehyde

https://huagongshe.com/reaction/1485057

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant(Bromomethyl)cyclobutaneHCID 2734658—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-(Cyclobutylmethoxy)benzaldehydeHCID 6545829176.4%

Reaction Steps

To a suspension of sodium hydride (60% dispersion in mineral oil, 0.328 g) in N,N-dimethylformamide (15.0 mL), a solution of 4-hydroxybenzaldehyde (1.00 g) in N,N-dimethylformamide (5.00 mL) was added at 0° C. and thereafter the mixture was stirred at room temperature for 30 minutes. After adding (bromomethyl)cyclobutane (1.22 g), the mixture was stirred at 70° C. for 24 hours. After cooling the reaction mixture to room temperature, 0.5 mol/L hydrochloric acid was added under cooling with ice and three extractions were conducted with ethyl acetate. The combined organic layers were passed through a phase separator and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=95:5-40:60) to give the titled compound as a colorless oil (1.19 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422240B2
Source datasetuspto-grants-2016_08
ORD IDord-793f93a6b864458891ae36d53bd1b4f9
Source noteuspto-grants-2016_08