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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxyphenol | HCID 9015 | — |
| Reactant | 2-(2-Tert-butoxy-2-oxoethylthio)ethyl methacrylate | HCID 14958442 | — |
| Reactant | chloroform methanol HOAc | HCID 21866353 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 2-(2-(Methacryloyloxy)ethylthio)acetic acid | HCID 14958453 | 63.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09339554B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-2af74332a52e455dbfbe09f3f66c82a3 |
|---|
| Source note | uspto-grants-2016_05 |
|---|