HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → Acetic acid, (2-iodophenoxy)-, ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 2-Iodophenol | HCID 10784 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Acetic acid, (2-iodophenoxy)-, ethyl ester | HCID 11808921 | 79% |
Reaction Steps
To a solution of 2-iodophenol (1 g, 4.55 mmol) in CH3CN (20 mL) was added K2CO3 (0.93 g, 6.83 mmol) and ethyl 2-bromoacetate (0.835 g, 5.0 mmol). The reaction mixture was stirred at reflux for 2 h, cooled to room temperature, extracted with EtOAc, washed with brine, dried over sodium sulfate and concentrated. The crude product was used in the next step without further purification. (1.1 g, yield 79%) MS (ESI+) e/z: 307.1 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365555B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-d1058cef8dfb4de7bb88da395c740b44 |
| Source note | uspto-grants-2016_06 |