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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275555Generated: October 30, 2026

Triethylamine → HCID 178442503, compound

https://huagongshe.com/reaction/275555

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): δ1.13(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 numberUS05393732
Source datasetuspto-grants-1995_02
ORD IDord-fdd63e9fd968417c84b8572e213f854b
Source noteuspto-grants-1995_02