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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210535Generated: November 1, 2026

Bromocyclopentane → 3-Cyclopentyloxy-4-methoxybenzaldehyde

https://huagongshe.com/reaction/2210535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromocyclopentaneHCID 8728—
ReactantPotassium CarbonateHCID 11430—
ReactantIsovanillinHCID 12127—
SolventDimethylformamideHCID 6228—
Product3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 2735893—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a magnetically-stirred solution of isovanillin (557 mmol, 85.0 g) in dry DMF (500 mL) at room temperature was added powdered K2CO3 (558 mmol, 77.1 g) in one portion followed by the dropwise addition of neat cyclopentyl bromide (614 mmol, 91.5 g; 65.9 mL). The resulting suspension was warmed to 60° C. and the reaction monitored by TLC until complete. Upon completion, the reaction mixture was cooled to room temperature and the DMF was removed in vacuo. The residue was partitioned between H2O and EtOAc, the aqueous phase extracted with EtOAc and the combined organic layers were washed with H2O. The organics were dried (Na2SO4) and concentrated in vacuo to afford the alkylated product (317 mmol, 70.1 g; 57%) as a viscous oil which was of sufficient purity to be used as such in subsequent transformation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05459151
Source datasetuspto-grants-1995_10
ORD IDord-2b301a8ac81f4312b8e519eac1b20d1e
Source noteuspto-grants-1995_10