Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489888Generated: October 23, 2026

9-Anthracenecarboxylic acid → Anthracene-9-carbonyl chloride

https://huagongshe.com/en/reaction/489888

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-Anthracenecarboxylic acidHCID 2201—
ReactantChloroformHCID 6212—
SolventThionyl ChlorideHCID 24386—
ProductAnthracene-9-carbonyl chlorideHCID 16752859%

Reaction Steps

Anthracene-9-carboxylic acid (recrystallized from ethanol, 12.05 g, 54.3 mmol) was suspended in a mixture of chloroform (60 mL, Aldrich, amylenes-stabilized) and thionyl chloride (12 mL) and heated under reflux until a clear solution was obtained (about 30 minutes). The solvent was removed by distillation under reduced pressure and the residual hot oil was dissolved in toluene (20 mL) and hexane (100 mL) was added. After cooling to ambient temperature the crystalline product was collected by filtration and dried in a stream of nitrogen then under high vacuum to give the title compound as a yellow solid (7.69 g, 59%). Non-commercially available carboxylic acids referred to in this section were prepared as described below. If desired they were converted to the corresponding carbonyl chloride using thionyl chloride as described above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06979741B2
Source datasetuspto-grants-2005_12
ORD IDord-6d6df2e26fae423f9920d14f54d9331b
Source noteuspto-grants-2005_12