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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003635Generated: October 30, 2026

Dichloromethane → HCID 15389066, compound

https://huagongshe.com/reaction/1003635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 15389065HCID 15389065—
SolventWaterHCID 962—
ProductHCID 15389066HCID 15389066—

Reaction Steps

2.2 g (4.7 mmol) of 4-{3-Hydroxy-3-[3,5-di-tert-butyl-4-(2-trimethylsilylethoxymethoxy)phenyl]-1-propynyl}benzoic acid and 75 ml of dichloromethane are introduced into a three-necked flask. 360 μl (4.7 mmol) of trifluoroacetic acid are added at -78° C. and the mixture is allowed to return to room temperature. The reaction medium is poured into water and extracted with ethyl ether, and the organic phase is separated out after settling has taken place, dried over magnesium sulphate and evaporated. The residue obtained is triturated from heptane, filtered and then dried. 1.6 g (90%) of 4-[3-(3,5-di-tert-butyl-4-oxo-2,5cyclohexadien-1-ylidene)-1-propynyl]benzoic acid are collected, with a melting point of 216-8° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046220
Source datasetuspto-grants-2000_04
ORD IDord-2229754ff1354c94833b411af63c4496
Source noteuspto-grants-2000_04