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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045085Generated: October 30, 2026

Butyric Acid → 5-Norbornene-2-carboxylic acid

https://huagongshe.com/reaction/1045085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyric AcidHCID 264—
ReactantTolueneHCID 1140—
CatalystZirconium, tetrakis(acetylacetonato)-HCID 5463922—
Product5-Norbornene-2-carboxylic acidHCID 7894989%

Reaction Steps

and 25 ml of toluene were continuously added to the 250 ml flask. Zirconium acetyl acetonate [Zr(acac)4] (0.658 g, 0.135 mmol, 1 mol %) was added thereto, and azeotropic reflux was performed. The temperature of the heated bath was controlled to 150° C. and the reaction was performed for 18 hours. After that, the reaction was finished after the GC check, and it was cooled to normal temperature. Thereafter, 30 mlm of ethyl acetic acid was added thereto. After the undissolved solid compound is precipitated, 30 ml of 1 M (mol/L) dilute hydrochloric acid solution was added thereto, and the washing was performed. This process was performed twice, and 30 ml of the saturated aq.NaHCO3 solution was added thereto and washed. This process was performed twice, and MgSO4 was added to the separated organic solution to remove a small amount of water. After water was removed, this was filtered by using MgSO4, and the solvent was removed under reduced pressure. The purification process was carried out to obtain 4.15 g of the compound (molecular weight=342.15, yield 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563764B2
Source datasetuspto-grants-2013_10
ORD IDord-9622d8cd6f2642f9a97a883a1e6d5b2e
Source noteuspto-grants-2013_10