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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585557Generated: November 2, 2026

1-Propanol → 2-Cyclopentyloxy-benzaldehyde

https://huagongshe.com/reaction/1585557

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 refluxed 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 IN 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 numberUS05939422
Source datasetuspto-grants-1999_08
ORD IDord-3ed661963d4d4676aa5d421bfc66bcea
Source noteuspto-grants-1999_08