HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383245Generated: October 29, 2026
Boron trifluoride etherate → HCID 57814383, compound
https://huagongshe.com/reaction/2383245
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 66933810 | HCID 66933810 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57814383 | HCID 57814383 | — |
Reaction Steps
12.6 mmol of sodium borohydride are suspended in 6 ml of tetrahydrofuran. 19.1 mmol of boron trifluoride ethyl etherate are added dropwise at 0° C. and the reaction mixture is stirred thoroughly for 10 minutes. A suspension of 1.27 mmol of 8-(4-methylsulphanylphenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridin-8-ol in 6 ml of tetrahydrofuran is added and the reaction mixture is stirred at room temperature for 16 hours. The reaction mixture is subsequently poured into saturated aqueous sodium hydrogen carbonate solution and extracted with dichloromethane (3×). The combined organic phases are dried with sodium sulphate and evaporated. From the residue the title compound is obtained by means of flash chromatography (SiO2 60 F) as a white solid. Rf=0.63 (dichloromethane/methanol 9:1); Rt=5.73 (Gradient I).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08263615B2 |
|---|
| Source dataset | uspto-grants-2012_09 |
|---|
| ORD ID | ord-dd2d59b81fba4ce49c19c770592e2819 |
|---|
| Source note | uspto-grants-2012_09 |
|---|