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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662991Generated: October 29, 2026

Triethylamine → HCID 67434957, compound

https://huagongshe.com/reaction/1662991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(But-3-en-1-yloxy)benzene-1-sulfonyl chlorideHCID 21884792—
ReactantHCID 67434472HCID 67434472—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67434957HCID 67434957—

Reaction Steps

To a solution of 2 g (7.683 mmol) of (4-[1,2,4]triazol-1-yl-benzylamino)-acetic acid ethyl ester in 15 ml of dioxane and 15 ml of H2O, 2.3 g (9.22 mmol) of 4-but-3-enyloxy-benzenesulfonyl chloride and 1.3 ml (9.22 mmol) of triethyl amine are successively added at 0-5° C. After being stirred for 18 h at r.t., the reaction mixture is diluted with H2O and extracted with AcOEt. The combined extracts are washed with brine, dried over MgSO4 and concentrated under reduced pressure. The residue is purified by column chromatography on silica gel to give the title compound. 1H-NMR (400 MHz, CDCl3): 1.17 (t, 3H, J=7.04 Hz), 2.55-2.65 (m, 2H), 3.95 (s, 2H), 4.07 (t, 2H, J=7.04 Hz), 4.09 (t, 2H, J=6.56 Hz), 4.53 (s, 2H), 5.10-5.25 (m, 2H), 5.85-5.95 (m, 1H), 6.99 (d, 2H, J=8.04 Hz), 7.44 (d, 2H, J=7.56 Hz), 7.64 (d, 2H, J=8.04 Hz), 7.82 (d, 2H, J=7.56 Hz), 8.11 (s, 1H), 8.55 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034810B2
Source datasetuspto-grants-2011_10
ORD IDord-87af44e879034708b81da6608dd215e5
Source noteuspto-grants-2011_10