Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523618Generated: October 26, 2026

4-Methoxyphenol → 2-(2-(Methacryloyloxy)ethylthio)acetic acid

https://huagongshe.com/reaction/523618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxyphenolHCID 9015—
Reactant2-(2-Tert-butoxy-2-oxoethylthio)ethyl methacrylateHCID 14958442—
Reactantchloroform methanol HOAcHCID 21866353—
SolventTrifluoroacetic acidHCID 6422—
Product2-(2-(Methacryloyloxy)ethylthio)acetic acidHCID 1495845363.6%

Reaction Steps

3 (2 g, 7.7 mmol, 1 eqv.) was slowly dissolved in trifluoroacetic acid (TFA) (10 mL) on ice under nitrogen. A trace amount of hydroquinone monomethyl ether (MEHQ) was added to the reaction mixture to prevent polymerisation. The reaction mixture was allowed to warm to room temperature and the reaction mixture was stirred for 2 hours at 55 C. Completion of the reaction was monitored by TLC(CHCl3/MeOH/HOAc, 9:1:0.1 (v/v), Rf: 0.17). Excess of TFA was removed by evaporation and coevaporation with CH2Cl2 and the residue was purified on a silica gel column (Hex/EtOAc, 4:1 (v/v)). Pure 4 was dried with MgSO4 and filtered through Ø 185 mm whatman filter papers. The filtrate was concentrated in vacuo. 1 g (63% yield) 4 was obtained as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09339554B2
Source datasetuspto-grants-2016_05
ORD IDord-2af74332a52e455dbfbe09f3f66c82a3
Source noteuspto-grants-2016_05