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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734861Generated: November 4, 2026

Triethylamine → HCID 53891592, compound

https://huagongshe.com/reaction/1734861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(2-Oxo-2-phenylethyl)(triphenyl)phosphanium bromideHCID 197064—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 19966069HCID 19966069—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 53891592HCID 5389159266%

Reaction Steps

10 ml of a tetrahydrofuran suspension containing 152 mg (0.392 mmol) of N-(2-formyl-6-methoxymethylphenyl)-2-(9H-xanthen-9-yl)acetamide (prepared as described in Preparation 53), 199 mg (0.432 mmol) of phenacyltriphenylphosphonium bromide and 48 mg (0.471 mmol) of triethylamine was heated for 6 hours under reflux. At the end of this time, the mixture was allowed to return to room temperature. 4 ml of methanol were added, and then 155 mg (4.10 mmol) of sodium borohydride were gradually added to the mixture, which was then stirred for 1 hour. The reaction solution was then diluted with ethyl acetate, and washed several times with water. The solvent was removed by distillation under reduced pressure. The residue was subjected to column chromatography through 20 g of silica gel. Elution with a 4:1 by volume mixture of methylene chloride and ethyl acetate afforded 126 mg (yield 66%) of the title compound as crystals, melting at 204.5°-206.5° C. (after recrystallization from methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534529
Source datasetuspto-grants-1996_07
ORD IDord-e0716ca494b64405894bbe493a567d36
Source noteuspto-grants-1996_07