HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 24851925, compound → HCID 68767239, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 24851925 | HCID 24851925 | — |
| Reactant | 4-acetyl-3-chlorobenzonitrile | HCID 68613708 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68767239 | HCID 68767239 | — |
Reaction Steps
To a solution of 1.5 g of 4-acetyl-3-chlorobenzonitrile in 25 ml anhydrous THF is added 158 mg sodium boron hybrid at 0° C. The ice bath is removed and the reaction mixture is stirred for 18 h at room temperature. The reaction mixture is poured into 90 ml of 1N aqueous HCl solution. The aqueous layer is extracted with ethyl acetate (3×50 ml). The combined organic layers are washed with a saturated solution of sodium chloride (100 ml), dried over MgSO4 and evaporated to dryness under reduced pressure. The remaining residue is purified by flash chromatography (n-hexane/ethyl acetate, 6/4 (v/v)) to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273890B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-b94d0f15a8d64573a27885ee1f9d833d |
| Source note | uspto-grants-2012_09 |