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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672594Generated: November 2, 2026

Water → HCID 66696611, compound

https://huagongshe.com/reaction/1672594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-difluoro-4-(trifluoromethyl)benzaldehydeHCID 5007468—
Reactant1-(1-Isocyanoethanesulfonyl)-4-methylbenzeneHCID 11052885—
SolventMethanolHCID 887—
ProductHCID 66696611HCID 6669661160%

Reaction Steps

A mixture of 1-(1-isocyanoethylsulfonyl)-4-methylbenzene (1 0.0 g, 47.8 mmol), 2,3-difluoro-4-(trifluoromethyl)benzaldehyde (9.68 g, 46.1 mmol), and K2CO3 (13.1 g, 95.0 mmol) in MeOH (240 mL) was heated to reflux. After 2 hr, the reaction mixture was cooled to ambient temperature, water (700 mL) was added, and the product was extracted with EtOAc (700 mL). The organic layer was washed with brine and dried over Na2SO4, filtered, and concentrated to an orange oil. The crude product was purified by chromatography on silica gel in five batches (Analogix® SF40-240G column, 100% CH2Cl2, 65 mL/min) to afford 7.22 g (60%) of the title compound as a light yellow liquid. 1H NMR (300 MHz, DMSO-d6) δ 8.56 (s, 1H), 7.78-7.69 (m, 1H), 7.68-7.59 (m, 1H), 2.30 (d, J=2.5, 3H). MS (DCI+) m/z 264 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998993B2
Source datasetuspto-grants-2011_08
ORD IDord-bc362eacbf8b4dda92053b4ffbe10594
Source noteuspto-grants-2011_08