HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-hydroxyphenylacetate → Ethyl 3-chloro-4-hydroxyphenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-hydroxyphenylacetate | HCID 28310 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 3-chloro-4-hydroxyphenylacetate | HCID 11031224 | 116.5% |
Reaction Steps
To a 0° C. solution of ethyl 2-(4-hydroxyphenyl)acetate (5.0 g, 0.02 mol) in THF (100 mL) was added NCS (4.45 g, 0.03 mol). The reaction mixture was then stirred at RT for 16 h and then extracted with EtOAc (2×200 mL). The combined organic layers were washed with water, dried over Na2SO4, and concentrated in vacuo to afford ethyl 2-(3-chloro-4-hydroxyphenyl)acetate (5 g, 84%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08481534B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-13d2883cdca440ea932d2827a5afb064 |
| Source note | uspto-grants-2013_07 |