HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → Ethyl [4-(bromoacetyl)phenyl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Ethyl 4-acetylphenylacetate | HCID 73716 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl [4-(bromoacetyl)phenyl]acetate | HCID 13027344 | 99% |
Reaction Steps
Ethyl 4-acetyl-phenylacetate from Example 25 Part A (489 mg, 2.4 mmol) was dissolved in CH2Cl2. Bromine (379 mg, 2.4 mmol) was added dropwise. The reaction was stirred at rt for 16 h. The reaction had decolorized from rust red to light yellow. The solvent was evaporated in vacuo to yield 680 mg (99%) of ethyl 2-(4-(2-bromoacetyl)phenyl)acetate as a light yellow oil. The product was used in the next step without further purification. MS 287.0 and 289.0 of equal intensities (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09079860B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-851e02e65fe6441f9e82f6a976a9e71b |
| Source note | uspto-grants-2015_07 |