HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Tetrachloride → Ethyl 3-bromo-6-methoxy-2-methylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-Methoxy-6-methyl-benzoic acid ethyl ester | HCID 591060 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 3-bromo-6-methoxy-2-methylbenzoate | HCID 11022052 | — |
Reaction Steps
A mixture of ethyl 6-methyl-2-methoxybenzoate (8.4 g, 43.2 mmol), bromine (6.9 g, 43.2 mmol) and tetrachloromethane (170 ml) is stirred at room temperature for 60 hours. The reaction mixture is poured into water and extracted with ethyl acetate. The organic phase is separated and concentrated. The crude product is obtained as a yellow oil, 10.3 g (87% y) and is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05945567 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-764df8cc1a0c436faa7522f56ba7521e |
| Source note | uspto-grants-1999_08 |