HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 5-(Methylsulfonyl)[1,1'-biphenyl]-2-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | 5-(Methylsulfonyl)biphenyl-2-carboxylic acid methyl ester | HCID 66968726 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(Methylsulfonyl)[1,1'-biphenyl]-2-methanol | HCID 117942038 | — |
Reaction Steps
To a solution of CaCl2 (1.52 g, 13.78 mmol) in EtOH (50 mL) at RT was added methyl 5-(methylsulfonyl)-[1,1′-biphenyl]-2-carboxylate (2 g, 6.9 mmol) in THF (50 mL) followed by the addition of NaBH4 (1.0 g, 27.6 mmol). The reaction was stirred at RT for 24 h, then concentrated in vacuo and extracted with ethyl acetate, 5% HCl, and brine. Purification on normal phase silica gel provided (5-(methylsulfonyl)-[1,1′-biphenyl]-2-yl)methanol as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09199994B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-fb349101b30e4bd7adc3eb33c00626e1 |
| Source note | uspto-grants-2015_12 |