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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191550Generated: November 1, 2026

[3-(4'-Chloro-4-methylbiphenyl-3-yl)-1,1-dimethylprop-2-ynyloxy]acetic acid → 6-[1-(4'-Chloro-4-methylbiphenyl-3-yl)methylidene]-5,5-dimethyl-[1,4]dioxan-2-one

https://huagongshe.com/reaction/1191550

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[3-(4'-Chloro-4-methylbiphenyl-3-yl)-1,1-dimethylprop-2-ynyloxy]acetic acidHCID 58312423—
CatalystHCID 178418647HCID 178418647—
SolventAcetonitrileHCID 6342—
Product6-[1-(4'-Chloro-4-methylbiphenyl-3-yl)methylidene]-5,5-dimethyl-[1,4]dioxan-2-oneHCID 6707294283.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

Silver carbonate (0.17 g, 0.61 mmol) is added to a solution of [3-(4′-chloro-4-methyl-biphenyl-3-yl)-1,1-dimethylprop-2-ynyloxy]acetic acid (2.1 g, 6.13 mmol) in anhydrous acetonitrile (15 ml) in a microwave vial. The reaction mixture is stirred and heated to 120° C. for 40 minutes under microwave irradiation to give a brown suspension. The mixture is evaporated in vacuo, then diluted with water and extracted with ethyl acetate. The combined organic extracts are dried over anhydrous sodium sulfate, filtered and the filtrate evaporated in vacuo to give 6-[1-(4′-chloro-4-methylbiphenyl-3-yl)methylidene]-5,5-dimethyl-[1,4]dioxan-2-one (1.75 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680012B2
Source datasetuspto-grants-2014_03
ORD IDord-6a5aac0a0b724decad3c18f3ac7e67a5
Source noteuspto-grants-2014_03