Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597298Generated: November 4, 2026

1-Propanol → 2-Cyclopentyloxy-benzaldehyde

https://huagongshe.com/reaction/1597298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PropanolHCID 1031—
ReactantIsovanillinHCID 12127—
ReactantPotassium tert-butoxideHCID 23665647—
Product2-Cyclopentyloxy-benzaldehydeHCID 315272377.5%

Reaction Steps

77.70 g (500 mmoles) of isovanillin and 69.40 g (600 mmoles) of 97% potassium t-butoxide (t-BuOK) dissolved in 800 ml of 1-propanol, 69.0 ml 630 mmoles), and the solution refluxed. After 3 hours another 9.25 g (80 mmoles) of t-BuOK were added at 80° C. and the suspension refined for another 3 hours. The solid was filtered off and the filtrate evaporated in vacuo to dryness. The residue was dissolved in ether and extracted with 1N NaOH. The ether phase was evaporated to dryness: 85.40 g (77.5%) of cyclopentyloxybenzaldehyde was isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06294541B1
Source datasetuspto-grants-2001_09
ORD IDord-bec6ffbb5c1c4e3d9cd950fda28d4013
Source noteuspto-grants-2001_09