HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Methanesulfonylbenzoic acid → (3-Methanesulfonylphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Methanesulfonylbenzoic acid | HCID 220380 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Methanesulfonylphenyl)methanol | HCID 23549738 | 90.2% |
Reaction Steps
A solution of 3-(methylsulfonyl)benzoic acid (1.0 g, 5.0 mmol) in anhydrous THF (25 mL) was treated with BH3.THF (1 M solution, 7.5 mL) at room temperature. The reaction was stirred for 12 hours before it was quenched by slow addition of MeOH. The solvent was removed and the residue was purified by flash column chromatography (0-5% MeOH in CH2Cl2) to give the product (0.84 g, 90% yield). 1H NMR (300 MHz, CDCl3) δ: 3.06 (s, 3H), 4.81 (d, J=6.0 Hz, 2H), 7.54-7.59 (m, 1H), 7.65-7.68 (m, 1H), 7.85-7.88 (m, 1H), 7.96 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07473790B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-4835e6c8a7834e3cad59f2d0a0a29f49 |
| Source note | uspto-grants-2009_01 |