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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272697Generated: October 26, 2026

4-Methyl-5-(2-hydroxyethyl)thiazole → 4-[2-(4-Methyl-1,3-thiazol-5-yl)ethoxy]-2-nitroaniline

https://huagongshe.com/reaction/272697

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-5-(2-hydroxyethyl)thiazoleHCID 1136—
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactant4-Amino-3-NitrophenolHCID 3758882—
SolventTetrahydrofuranHCID 8028—
Product4-[2-(4-Methyl-1,3-thiazol-5-yl)ethoxy]-2-nitroanilineHCID 6921998386.2%

Reaction Steps

A mixture of 4-amino-3-nitrophenol (386 mg, 2.5 mmol), 2-(4-methyl-1,3-thiazol-5-yl)ethanol (0.299 mL, 2.5 mmol), polymer supported triphenylphosphine (1.25 g, 3 mmol/g, 3.75 mmol), and di-tert-butyl azodicarboxylate (864 mg, 3.75 mmol) in THF (10 mL) was stirred at room temperature for 16 hours. Filtered through Celite and concentrated under vacuum. The residue was purified by flash column chromatography on silica gel with 1:1 hexanes/ethyl acetate to provide 602 mg (86%) of the desired product. MS (DCI) m/e 279 (M+H)+, 1H NMR (300 MHz, DMSO-d6): □ 8.83 (s, 1H), 7.37 (d, J=3.05 Hz, 1H), 7.25 (s, 2H), 7.16 (dd, J=8.99, 2.88 Hz, 1H), 7.01 (s, 1H), 4.10 (t, J=6.27 Hz, 2H), 3.19 (t, J=6.27 Hz, 2H), 2.35 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456169B2
Source datasetuspto-grants-2008_11
ORD IDord-409df72e33cf45d8a976a3b4eefceee5
Source noteuspto-grants-2008_11