Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351686Generated: November 3, 2026

2,4-Difluoroacetophenone → HCID 21099384, compound

https://huagongshe.com/reaction/1351686

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DifluoroacetophenoneHCID 67770—
Reactanto-FluorobenzaldehydeHCID 67970—
ReactantSodium borohydrideHCID 4311764—
ReactantSodiumHCID 5360545—
ReactantHCID 68534518HCID 68534518—
ProductHCID 21099384HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217740B2
Source datasetuspto-grants-2007_05
ORD IDord-e3c0dfb51b20470fbc35a75ed6faa5b0
Source noteuspto-grants-2007_05