HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → HCID 57743039, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 57743073 | HCID 57743073 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57743039 | HCID 57743039 | 35.6% |
Reaction Steps
Under argon, BBr3 (1M in CH2Cl2) (1.86 ml, 1.8645 mmol, 2 eq) is added drop wise to a solution of 1-[(2-chloro-6-methoxy-1H-benzimidazol-1-yl)methyl]-4-propylpyrrolidin-2-one 305 (0.3 g, 0.9322 mmol, 1 eq) in dry CH2Cl2 (20 ml). After 48 hours at room temperature, saturated aqueous solution of NaHCO3 (20 ml) is added. The aqueous layer is extracted with CH2Cl2 (3×20 ml) then the combined organic layers are dried on anhydrous MgSO4, filtered off and evaporated under reduced pressure. The remaining pale yellow solid is recrystallized in MeCN/H2O (9/1) to yield 102 mg of 1-[(2-chloro-6-hydroxy-1H-benzimidazol-1-yl)methyl]-4-propylpyrrolidin-2-one 320 as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08586623B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-bef00ac9a9894d13a26155f4e1d146ae |
| Source note | uspto-grants-2013_11 |