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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585599Generated: October 30, 2026

Dimethylformamide → HCID 22337835, compound

https://huagongshe.com/reaction/585599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant6-AminonaphtholHCID 90295—
Reactant4-(Chloromethyl)-5-methyl-2-phenyl-1,3-oxazoleHCID 9794289—
ProductHCID 22337835HCID 2233783530%

Reaction Steps

5-methyl-2-phenyl-4-Chloromethyloxazole (3.34 g) is added to a chilled mixture of 2-Amino-5-naphthol (2.55 g) and sodium hydride (0.65 g) in dimethylformamide (100 mL). Let stir overnight at room temperature. Concentrate in vacuo. Redilute with ethylacetate and absorb onto silica gel. Chromatograph (ethyl acetate/hexane) to give 2-amino-5-(methyl-2-phenyl-oxazol-4-ylmethoxy)naphthalene (1.59 g, 30%). Without further characterization this amine and triethylamine (0.67 mL) were dissolved in dichloromethane (75 mL). Cooled in an acetone and dry ice bath. Triflic anhydride (0.81 mL) was added and the mixture had warmed to room temperature overnight. Partition between water and ethyl acetate. Separate and dry with magnesium sulfate. Concentrate at rotovap, and triturate with ethyl acetate to provide the title compound (0.70 g, 30%) as a white solid, m.p. 192-194° C. 1H NMR (DMSO-d6, 400 MHz): δ 2.49 (s, 3H), 5.21 (s, 2H), 7.17 (d, 1H), 7.36 (d, 1H), 7.46-755 (m, 5H), 7.73 (s, 1H), 7.93-7.97 (m, 2H), 8.13 (d, 1H). MS [EI, m/z]: 462 [M]+. Anal. Calcd. for C22H17F3N2O4S 0.75(H2O): C, 55.52; H, 3.92; N, 5.89. Found: C, 55.62; H, 4.13; N, 5.45.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06933322B2
Source datasetuspto-grants-2005_08
ORD IDord-233a1ef688d34c35b56e9d34235f1977
Source noteuspto-grants-2005_08