HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Methyl 2-(3-bromophenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | (3-Bromophenyl)acetic acid | HCID 74653 | — |
| Product | Methyl 2-(3-bromophenyl)acetate | HCID 11746402 | — |
Reaction Steps
To a solution of 3-bromophenylacetic acid (10 g, 46 mmol) in CH2Cl2 (20 mL) was added CH2N2 (Et2O) until yellow coloration persisted. The resulting reaction mixture was quenched with AcOH, and diluted with a NaHCO3 solution and ethyl acetate. The organic extracts were washed (H2O, brine), dried (MgSO4), filtered and concentrated to provided the (3-Bromo-phenyl)-acetic acid methyl ester compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06919353B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-8f48685f14164b6f93b21ceb71f185f4 |
| Source note | uspto-grants-2005_07 |