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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13534Generated: October 26, 2026

Tetrahydrofuran → 4-Formylbenzoyl chloride

https://huagongshe.com/reaction/13534

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 numberUS07728129B2
Source datasetuspto-grants-2010_06
ORD IDord-11c8be357cc7419c80cf8a2b182ca001
Source noteuspto-grants-2010_06