HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632027Generated: October 31, 2026
Toluene → (3'-Chloro-2-fluoro-6-methoxy-biphenyl-3-yl)-methanol
https://huagongshe.com/reaction/1632027
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (3-Chlorophenyl)boronic acid | HCID 2734323 | — |
| Reactant | (3-Bromo-2-fluoro-4-methoxyphenyl)methanol | HCID 57703782 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (3'-Chloro-2-fluoro-6-methoxy-biphenyl-3-yl)-methanol | HCID 57703788 | 74.1% |
Reaction Steps
Into a 100 mL round bottom flask was added (3-bromo-2-fluoro-4-methoxy-phenyl)-methanol (I-31, 1.04 g, 4.0 mmol), 3-chlorophenylboronic acid (0.76 g, 4.8 mmol), Pd(PPh3)4 (0.45 g, 0.41 mmol), Na2CO3 (6 mL, 2M aq), toluene, (32 mL), and EtOH (11 mL). The reaction was degassed with N2, then stirred at 80° C. for 24 hours. Water was added and the product was extracted with ethyl acetate. The combined organics were concentrated and filtered through a SiO2 plug eluting with 50% ethyl acetate/hexanes. The solid was triturated with ether and filtered. The filtrate was concentrated and triturated with ether and filtered. The filter cakes were combined and purified by flash column chromatography eluting with 20% acetone/hexanes to give (3′-chloro-2-fluoro-6-methoxy-biphenyl-3-yl)-methanol (I-32, 0.79 g, 67%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08791267B2 |
|---|
| Source dataset | uspto-grants-2014_07 |
|---|
| ORD ID | ord-005c295a104b456bba38f83387c612e3 |
|---|
| Source note | uspto-grants-2014_07 |
|---|