HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590629Generated: October 30, 2026
Carbon Dioxide → 5-Bromothiophene-2-carboxylic acid
https://huagongshe.com/reaction/590629
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 2,5-Dibromothiophene | HCID 18453 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Bromothiophene-2-carboxylic acid | HCID 349115 | 57% |
Reaction Steps
THF (50 mL) was added via cannula to a flame-dried 100 mL Schlenk flask. 2,5-dibromothiophene (10 mmol, 2.42 g) was added via syringe. Reaction vessel was cooled to −78° C. and n-butyllithium (1.61M solution in hexanes, 11 mmol, 6.8 mL) was added dropwise over 5 minutes. The solution was allowed to stir at −78° C. for 1 hr. Dry ice (approx. 50 g) was added to the reaction mixture, and was allowed to stir and return to room temperature for 18 hrs. under nitrogen. The light gray suspension was filtered and the white solid was stirred in 2M HCl for 1 hr. The suspension was filtered to yield a white solid (5.7 mmol, 1.2 g, 57%). 1H NMR (400 MHz, CDCl3) δ: 11.45 (br s, 1H), 7.64 (d, 1H, J=4.0 Hz), 7.11 (dd, 1H, J=4.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09234003B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-34f37af4a65a4a4ea0816c6743d151af |
|---|
| Source note | uspto-grants-2016_01 |
|---|