HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 2-Fluoro-3-(hydroxymethyl)-6-iodobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Fluoro-3-formyl-6-iodobenzonitrile | HCID 86019349 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Fluoro-3-(hydroxymethyl)-6-iodobenzonitrile | HCID 66681189 | 63% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of Example 220A (5.0 g, 18 mmol) in MeOH (100 mL) at 0° C. was treated with NaBH4 (822 mg, 22 mmol) and the mixture was stirred for 1 h at 0° C. Acetone was added and the mixture was stirred for 5 min, then concentrated to dryness. The residue was partitioned between H2O and EtOAc. The extracts were washed with brine, dried (MgSO4) and concentrated. The residue was purified by flash chromatography on silica gel, eluting with 3:2 hexanes/EtOAc to give the desired product (3.14 g). Rf=0.38 (3:2 hexane:EtOAc).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642776B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-186942ce403c40e491f3e82299385f69 |
| Source note | uspto-grants-2014_02 |