HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Dichlorobenzylic alcohol → 2,6-Dichloro-2′,4′-difluoro[1,1′-biphenyl]-4-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Dichlorobenzylic alcohol | HCID 43236 | — |
| Reactant | 2,4-Difluorophenylboronic acid | HCID 2734334 | — |
| Reactant | HCID 66764840 | HCID 66764840 | — |
| Product | 2,6-Dichloro-2′,4′-difluoro[1,1′-biphenyl]-4-methanol | HCID 67471303 | 72.5% |
Reaction Steps
Using essentially the same coupling procedure as for Example 8-1, Step 1, but heating 2,4-difluorophenylboronic acid (456 mg, 2.89 mmol) and 3,5-dichloro-4-iodobenzyl alcohol (350 mg, 1.155 mmol) in a microwave at 115° C. for 120 minutes, afforded the title intermediate (242 mg) without formation of any appreciable 3,5-dichlorobenzyl alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08742110B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-4e5d3bee6e4b468ba2407a65071734d1 |
| Source note | uspto-grants-2014_06 |