HuagongsheHuagongshe Chemistry Print Report · For research reference only
Borane → (3-Methanesulfonylphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Borane | HCID 6331 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 3-Methanesulfonylbenzoic acid | HCID 220380 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Methanesulfonylphenyl)methanol | HCID 23549738 | — |
Reaction Steps
To a solution of 3-(methylsulfonyl)benzoic acid (1.2 g, 6.0 mmol) in THF (30 mL) at 0° C., is added equimolar amounts of borane (6.0 mL of a 1.0 M solution in THF) and boron trifluoride diethyl etherate (0.8 mL, 6.0 mmol). The reaction is allowed to warm to ambient temperature overnight, and then quenched by pouring into a mixture of ice and solid NaHCO3. Following extraction with EtOAc, the organic layer is washed with brine and dried over Na2SO4. Removal of solvent affords the product as a colorless oil: MS (M+NH4)+=204.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119666B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-daaa337f742940e68ed722cc107bfa3a |
| Source note | uspto-grants-2012_02 |