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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327380Generated: November 3, 2026

Benzoyl chloride → HCID 19108264, compound

https://huagongshe.com/reaction/327380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant1,4-Benzenediol, 2,6-diiodo-HCID 74775—
SolventPyridineHCID 1049—
ProductHCID 19108264HCID 19108264—
ProductHCID 54077011HCID 54077011—

Reaction Steps

To 2,6-diiodohydroquinone (0.2 g) in pyridine (10 mL) was added benzoyl chloride (0.140 mg) and the reaction mixture was stirred at room temperature for 1 hour. Following solvent removal in vacuo, purification was achieved by extraction (equal volumes ethyl acetate (EtOAc):0.01N HCl), and preparative TLC (methylene chloride) of the concentrated (in vacuo) EtOAc phases. Both the desired monoester, 4-hydroxy-2,6-diiodophenyl benzoate (Rf 0.38) and the diester, 3,5-diiodo-4(phenylmethanoyloxy)phenyl benzoate (Rf 0.96), products were formed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05273885
Source datasetuspto-grants-1993_12
ORD IDord-d9ecdf0fe41e4f7890a396d5b0c9fef3
Source noteuspto-grants-1993_12