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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227349Generated: October 30, 2026

1-Propanol → 2-Cyclopentyloxy-benzaldehyde

https://huagongshe.com/reaction/2227349

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 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 numberUS06413975B1
Source datasetuspto-grants-2002_07
ORD IDord-4e3f3970edc94e6e9c8dc563cecca0a1
Source noteuspto-grants-2002_07