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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715402Generated: October 31, 2026

N-(4-Chloro-3-hydroxymethyl-benzyl)-3,3,3-trifluoro-propionamide → N-(4-Chloro-3-formyl-benzyl)-3,3,3-trifluoro-propionamide

https://huagongshe.com/reaction/1715402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-Chloro-3-hydroxymethyl-benzyl)-3,3,3-trifluoro-propionamideHCID 67148258—
CatalystManganese dioxideHCID 14801—
SolventAcetonitrileHCID 6342—
ProductN-(4-Chloro-3-formyl-benzyl)-3,3,3-trifluoro-propionamideHCID 86622955100.5%

Reaction Steps

MnO2 (1.44 g, 14.9 mmol) was added to a sol. of N-(4-chloro-3-hydroxymethyl-benzyl)-3,3,3-trifluoro-propionamide (841 mg, 2.99 mmol) in CH3CN (60 mL). The mixture was stirred at rt for 3 h. MnO2 (1.44 g, 14.9 mmol) was added again, and the mixture was stirred for 90 min. The mixture was filtered over Celite, and the precipitate was washed with CH3CN and CH2Cl2. The solvents were removed under reduced pressure, and the residue was dried under high vacuum, yielding the crude title compound (840 mg, quantitative yield) that was used without purification. LC-MS: tR=0.84 min; ES+: 341.21.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799805B2
Source datasetuspto-grants-2010_09
ORD IDord-1a6706d383944ace904765e64c725408
Source noteuspto-grants-2010_09