HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354079Generated: October 29, 2026
Lithium Chloride → HCID 12992515, compound
https://huagongshe.com/reaction/354079
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 6-Methoxy-1-benzothiophene | HCID 13634237 | — |
| Reactant | Trifluoro-methanesulfonic acid benzothiazol-6-yl ester | HCID 54151956 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12992515 | HCID 12992515 | — |
Reaction Steps
A solution of 6-methoxybenzo[b]thiophene (300 mg, 1.82 mmol) in 5 mL of THF was cooled to −20° C. and 2.5 M n-BuLi (0.8 mL, 2.01 mmol) was added dropwise. The reaction was stirred at 0° C. for 0.5 hrs and then warmed to room temperature for an additional 0.5 hrs. Next a 0.5 M solution of anhydrous zinc chloride in THF (4.75 mL, 2.38 mmol) was added and the reaction was stirred at room temperature for 15 minutes followed by the addition of anhydrous lithium chloride (3 equivalents), tetrakis-triphenylphosphine palladium (84 mg, 0.073 mmol) and, by cannula, the product from Example 18, Step 1 (505 mg, 2.01 mmol) dissolved in 2 mL of THF. The reaction was stirred at room temperature for 16 hrs. The THF was removed and the residue diluted in water and extracted three times with Ethyl acetate. The combined organics were dried over anhydrous sodium sulfate, filtered, and concentrated. The crude material was chromatographed on silica gel using 1:20 THF/Hexanes to 1:10 THF/Hexanes as the gradient eluant to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06756388B1 |
|---|
| Source dataset | uspto-grants-2004_06 |
|---|
| ORD ID | ord-ce06b0776db14cef985096f19f983d58 |
|---|
| Source note | uspto-grants-2004_06 |
|---|