HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 2-Bromo-6-chlorobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 1-Bromo-3-chlorobenzene | HCID 7928 | — |
| Reactant | LDA THF ethylbenzene heptane | HCID 86590273 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-6-chlorobenzoic acid | HCID 33125 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
The mixture of 500 mg of 3-bromochlorobenzen and 3 ml of tetrahydrofuran was cooled down to −78° C. and 1.3 ml of 2.0M lithium diisopropylamide heptane/tetrahydrofuran/ethylbenzene was added. After stirring it for 2 hours, the mixture was put into dry ice and washed and extracted as described in Referencial Example 1 to obtain a crude material. The crude material was washed with a mixed solvent of hexane-ethyl acetate to obtain the said compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08426588B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-8f4e23bff75a4f7ebee43da1d721daa8 |
| Source note | uspto-grants-2013_04 |