Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714092Generated: October 31, 2026

Tetrahydrofuran → 4-Formylbenzoyl chloride

https://huagongshe.com/reaction/1714092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-Formylbenzoic acidHCID 12088—
ReactantOxalyl chlorideHCID 65578—
Product4-Formylbenzoyl chlorideHCID 12424620—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a thin suspension of 4-carboxybenzaldehyde (600 g, 3.92 mol) in tetrahydrofuran (2664 g, 36.57 mol) was added dimethylformadehyde (11.48 g, 0.16 mol) and the reaction mixture was cooled to 0-5° C. with an ice bath. The reaction mixture was then stirred at 0° C. while oxalyl chloride (608.69 g, 4.70 mol) was added slowly. The reaction mixture was stirred until it was deemed complete by 1HNMR to yield the title compound. The reaction mixture was used in the next step without further manipulation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795426B2
Source datasetuspto-grants-2010_09
ORD IDord-46c1ffa6aaeb47c9b9892576bdc2cd0f
Source noteuspto-grants-2010_09