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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361967Generated: October 26, 2026

Acetic Acid → 2,6-Dichloro-2',3'-dihydroxy-4'-methoxy-6'-methyl-benzophenone

https://huagongshe.com/reaction/361967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen BromideHCID 260—
Reactant2,6-Dichloro-2',3',4'-trimethoxy-6'-methyl-benzophenoneHCID 22719953—
SolventWaterHCID 962—
Product2,6-Dichloro-2',3'-dihydroxy-4'-methoxy-6'-methyl-benzophenoneHCID 54569551—

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of 2,6-dichloro-2',3',4'-trimethoxy-6'-methyl-benzophenone (1.78 g; 5 mmol) hydrobromic acid (7.5 ml; 30% in acetic acid) and acetic acid (7.5 ml) is stirred at 75° C. for 2 hours. Water is added and the mixture extracted with methylenechloride. The extract is washed with waterand shaken with 2N sodium hydroxide. The alcaline solution is acidified with hydrochloric acid, the separated compound dissolved in methylenechloride and the solution washed with water. After evaporation ofthe solvent purification is carried out by chromatography (flash column, filled with 36 g of silicagel; elution with 500 ml of petrolether/ethylacetate (4:1; v/v) and 250 ml of petrolether/ethylacetate(1:1; v/v)). the fraction containing the compound is concentrated, the compound crystallized. The yellow crystals are washed with petrolether andsucked off; 0.64 g (39% y), mp. 182° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866722
Source datasetuspto-grants-1999_02
ORD IDord-f2bc4d1e56aa4859abea606d965acb6e
Source noteuspto-grants-1999_02