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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162514Generated: October 29, 2026

2-Nitro-4-(trifluoromethyl)phenol → HCID 59520419, compound

https://huagongshe.com/reaction/1162514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitro-4-(trifluoromethyl)phenolHCID 9816—
ReactantCesium carbonateHCID 10796—
ReactantHCID 11051825HCID 11051825—
SolventAcetonitrileHCID 6342—
ProductHCID 59520419HCID 59520419—

Reaction Conditions

Temperature90 °C

Reaction Steps

2-nitro-4-trifluoromethyl-phenol 7 (4.1 g, 20 mmol) and methanesulfonic acid but-2-ynyl ester 20 (3.0 g, 20 mmol) are dissolved in MeCN. Cs2CO3 is added (13.0 g, 40 mmol) and the mixture is stirred at 90° C. for 12 hours. The mixture is then filtered, concentrated in vacuo, diluted with H2O and extracted three times with DCM. The organic layers are combined, dried (MgSO4), filtered, and concentrated and the remainder purified by column chromatography using a hexanes/EtOAc gradient to afford 1-but-2-ynyloxy-2-nitro-4-trifluoromethyl-benzene 21 as a yellow solid: 1H-NMR (400 MHz, CDCl3) δ=8.06 (d, J=1.7 Hz, 1H), 7.73 (dd, J=8.8 Hz, J=1.8 Hz, 1H), 7.30 (d, J=8.8 Hz, 1H), 4.81 (q, J=2.3 Hz, 2H), 1.79 (t, J=2.3 Hz, 3H). MS calculated for C11H9F3NO3 (M+H+) 260.1, found 260.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820705B2
Source datasetuspto-grants-2010_10
ORD IDord-d1b88a6cd57d43dbad13fa39d3231f90
Source noteuspto-grants-2010_10