HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Difluoroacetophenone → HCID 21099384, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Difluoroacetophenone | HCID 67770 | — |
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 68534518 | HCID 68534518 | — |
| Product | HCID 21099384 | HCID 21099384 | — |
Reaction Steps
2-Fluorobenzaldehyde was reacted with sodium 4-bromophhenylsulfinate by the procedure of Example 113 Step 1, then the aldehyde group reduced using sodium borohydride by the procedure of Example 41. The resulting bromophenylsulfonylbenzyl alcohol was reacted with 2′,4′-difluoroacetophenone as described in Example 132 to provide the title compound. δH (500 MHz, d6 DMSO): 8.07 (1H, d, J=7.8 Hz), 7.96 (1H, q, J=8.0 Hz), 7.82-7.77 (3H, m), 7.72 (1H, t, J=7.5 Hz), 7.54 (1H, t, J=7.5 Hz), 7.48 (2H, d, J=8.2 Hz), 7.45-7.41 (1H, m), 7.23 (1H, td, J=2.2, 7.7 Hz), 5.41 (1H, t, J=5.7 Hz), 4.69 (2H, d, J=5.7 Hz), 4.45 (2H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07468393B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-b88cf00542334daca45a232096d7617b |
| Source note | uspto-grants-2008_12 |