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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582173Generated: October 30, 2026

Triethylamine → HCID 178442503, compound

https://huagongshe.com/reaction/582173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTributylphosphineHCID 13831—
ReactantBromineHCID 24408—
ReactantHCID 178444075HCID 178444075—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 178442503HCID 17844250375.3%

Reaction Steps

A solution of bromine (0.53 g) in dichloromethane (1 ml) was added dropwise to a solution of tri-n-butylphosphine (0.68 g) in dichloromethane (12 ml), whilst maintaining the temperature below 0° C. The mixture was stirred for ten minutes at this temperature then treated, dropwise with stirring, with a solution of diethyl 3-hydroxy-3(1-trityl-1,2,4-triazol-3-yl)propane phosphonate (1.5 g, prepared as described in Example 24) and triethylamine (0.30 g) in dichloromethane (20 ml), maintaining the temperature below 0° C. It was allowed to warm slowly to room temperature, to stand for two days, then diluted with ethyl acetate, washed with water and brine, dried over magnesium sulphate and evaporated under reduced pressure. The residue was chromatographed on silica, using dichloromethane-ethanol (49:1) as eluant, to give diethyl 3-bromo-3(1-trityl-1,2,4-triazol-3-yl)propane phosphonate (1.27 g, m.p. 108-110° C.). NMR (CDCl3): δ 1.13(6H,dt), 1.6-2.1(2H,m), 2.5-2.6(2H,m), 4.1(4H,m), 5.15(1H,t), 7.1(6H,m), 7.3(9H,m), 7.9(1H,s). M/S: M+ 567,569.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922644
Source datasetuspto-grants-1999_07
ORD IDord-5817be4a888b40d09512a664c4442e5d
Source noteuspto-grants-1999_07