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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376983Generated: October 30, 2026

Benzaldehyde → HCID 21099482, compound

https://huagongshe.com/reaction/2376983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantMethyl morpholine oxideHCID 82029—
Reactant3-[[4-[2-(2,4-Difluorophenyl)ethyl]phenyl]sulfonyl]benzenemethanolHCID 21099483—
CatalystHCID 178419074HCID 178419074—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 21099482HCID 2109948268%

Reaction Steps

To a solution of [3-({4-[2-(2,4-difluorophenyl)ethyl]phenyl]sulfonyl)phenyl]methanol (prepared from 3-({4-[E)-2-(2,4-difluorophenyl)vinyl]phenyl}sulfonyl)benzaldehyde (Example 50 Step 1) according to the method of Example 117) in dichloromethane (4 mL) was added 4 Å molecular sieves (0.1 g) and the mixture stirred for 10 minutes. 4-Methylmorpholine N-oxide (68 mg, 0.58 mmol) was added in one portion and the reaction stirred for 10 minutes, then tetrapropylammonium perruthenate (6.9 mg, 0.02 mmol) added. The reaction was stirred for 30 minutes then diluted with ethyl acetate, filtered through a pad of silica and washed with further ethyl acetate. The filtrate was evaporated in vacuo. The residue was purified by flash column chromatography on silica, eluting with 25% ethyl acetate/isohexane, to yield 3-({4-[2-(2,4-difluorophenyl)ethyl]phenyl)sulfonyl)benzaldehyde (103 mg, 68%). δH (400 MHz, CDCl3): 10.06 (1H, s), 8.40 (1H, s), 8.18 (1H, d, J=7.8 Hz), 8.07 (1H, d, J=7.6 Hz), 7.87 (2H, d, J=8.3 Hz), 7.69 (1H, t, J=7.7 Hz), 7.30 (2H, d, J=8.2 Hz), 6.99 (1H, q, J=7.9 Hz), 6.79-6.73 (2H, m), 2.95-2.87 (4H, m). m/z (ES+) 387 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468393B2
Source datasetuspto-grants-2008_12
ORD IDord-67bc646a7b544a44a866267321f4432c
Source noteuspto-grants-2008_12