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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861426Generated: October 31, 2026

Diphenyl Ether → HCID 136061494, compound

https://huagongshe.com/reaction/861426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenyl EtherHCID 7583—
ReactantHCID 19703130HCID 19703130—
SolventDiethyl EtherHCID 3283—
ProductHCID 136061494HCID 136061494—

Reaction Steps

5-(4-allyloxyphenyl)-3-methyl-1,2,4-oxadiazole (1.2 g) and diphenyl ether (5 ml) were warmed gently to give a solution. This stirred solution, under an atmosphere of argon, was immersed in an oil bath at 265° C. for 12 minutes. This procedure was repeated three times. The deep red solutions were combined, diluted with diethyl ether (100 ml) and extracted with aqueous 1M sodium hydroxide (3×20 ml). The alkaline extracts were combined, washed with ether (3×30 ml), cooled in ice-water, acidified with aqueous 5M hydrochloric acid (15 ml), and extracted with ether (3×60 ml). The ether extracts were combined, washed with saturated brine (25 ml), dried (Na2SO4) and evaporated. The residue was purified by flash column chromatography on silica gel using 20% ethyl acetate/n-pentane as eluent, to give 2-allyl-4-(3-methyl-1,2,4-oxadiazol-5-yl)phenol as a solid m.p. 135°-137° C.; microanalysis, found: C, 66.7; H, 5.8; N, 12.5%; C12H12N2O2 requires: C, 66.7; H, 5.6; N, 13.0%; NMR: 2.3-2.35(3H,s), 3.3-3.4(2H,d), 5.0-5.15(2H,m), 5.85-6.1(1H,m), 6.95-7.05(1H,d), 7.75-7.8(2H,m) and 10.4-10.5(1H,s); m/z 217 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05714496
Source datasetuspto-grants-1998_02
ORD IDord-3688d9c85d8141a38d38e34e8ad81a1a
Source noteuspto-grants-1998_02