HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Difluorobenzaldehyde → HCID 57835854, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Difluorobenzaldehyde | HCID 588160 | — |
| Reactant | HCID 178419637 | HCID 178419637 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57835854 | HCID 57835854 | 88.9% |
Reaction Steps
4-(2-Tetrahydro-2H-pyranoxy)phenylmagnesium bromide (0.5 M in THF, 35 mL, 17.5 mmol) was added to a solution of 3,5-difluorobenzaldehyde (1.95 g, 13.7 mmol) in THF (50 mL) slowly via syringe at −78° C. The reaction mixture was stirred at this temperature for 3 hours and then quenched with saturated NH4Cl (aqueous). The mixture was extracted with EtOAc (60 mL×2), and the combined organic layers were dried over Na2SO4, filtered, and concentrated under reduced pressure to provide a colorless oil (3.9 g) as product M6.1, which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07582803B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-794e9aad03d94c37a549e78a59620378 |
| Source note | uspto-grants-2009_09 |