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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606183Generated: October 31, 2026

Trichloroacetic Acid → Trichloroacetic Acid

https://huagongshe.com/reaction/1606183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetic AcidHCID 6421—
Reactant1-Chloro-4-iodosylbenzeneHCID 22134080—
SolventDichloromethaneHCID 6344—
ProductTrichloroacetic AcidHCID 6421—
ProductHCID 21546139HCID 21546139—

Reaction Steps

A quantity of 135 g. (0.53 mole) p-chloroiodosobenzene is suspended in 800 ml. of methylene chloride contained in a 2-liter Erlenmeyer flask. To the suspension is added 190 g. (1.16 mole) trichloroacetic acid dissolved in 500 ml. of methylene chloride with agitation over a 5-minute period, the reaction temperature being maintained at room temperature. After 30 minutes, the solution is filtered and solvent is removed under reduced pressure. The solid residue is triturated with ether and filtered. The solid is collected on the filter, washed with ether and dried. The slightly off-white crystalline solid thereby obtained melts with decomposition at 155°-157°C. The yield is 80-85%. The carbon, hydrogen and iodine analyses and infrared spectra are consistent with the named structure. The substitution of dichloroacetic acid for trichloroacetic acid gives the corresponding 4-chloro-bis(dichloroacetoxy)iodobenzene which melts at 111°-112°C. with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952028
Source datasetuspto-grants-1976_04
ORD IDord-93cbc3a98a184bb288fd3ac0de093bd4
Source noteuspto-grants-1976_04