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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378668Generated: November 1, 2026

N-(4,5-Difluoro-2-(hydroxymethyl)phenyl)pivalamide → N-(4,5-Difluoro-2-formylphenyl)pivalamide

https://huagongshe.com/reaction/2378668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4,5-Difluoro-2-(hydroxymethyl)phenyl)pivalamideHCID 59732039—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
ProductN-(4,5-Difluoro-2-formylphenyl)pivalamideHCID 5973200826%

Reaction Steps

Pyridiniumchlorochromate (9.36 g, 43.4 mmol) was added to the solution of the crude N-(4,5-difluoro-2-(hydroxymethyl)phenyl)pivalamide in CH2Cl2 (150 mL) at rt. The yellow solution turned into dark brown in 10 min, and the mixture was continued stirring for 3 hr, and then passed through a thin silica gel pad with CH2Cl2 (2×50 mL). The combined organic solution was concentrated on rotary vacuum, and purified on flash chromatography eluting with 20˜60% EtOAc/hexanes(1300 mL) to afford the expected product as a brown solid(1.91 g, 26% yield after three step); 1H NMR (400 MHz, CDCl3) δppm 1.29 (s, 9H), 7.42-7.48 (m, 1H), 8.75 (dd, J=13.35, 7.30 Hz, 1H), 9.77-9.80 (m, 1H), 11.40 (s, 1H); Mass spec. 242.08 (MH+), Calc. for C12H13F2NO2 241.09.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470679B2
Source datasetuspto-grants-2008_12
ORD IDord-6c7646df7d30473cbcd6483f20f68f74
Source noteuspto-grants-2008_12