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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757785Generated: October 28, 2026

Benzyl Alcohol → HCID 54488810, compound

https://huagongshe.com/reaction/1757785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant3,5-Bis[(1-oxodecyl)amino]benzoic acidHCID 15232832—
SolventTolueneHCID 1140—
ProductHCID 54488810HCID 5448881045.3%

Reaction Steps

To a suspension of 5.0 g (10.85 mmol) of 3,5-bis[(1-oxodecyl)amino]benzoic acid in 150 ml of anhydrous toluene cooled in an ice bath and stirred under an argon atmosphere was added 2.8 ml (13.0 mmol) of diphenylphosphoryl azide followed by 1.8 ml (13.0 mmol) of triethylamine. The reaction mixture was stirred in the ice bath for 1.5 hours, at room temperature for 1 hour and then at 90° for 2 hours. Benzyl alcohol (39 ml, 0.38 mol) was added and heating at 90° was continued for 4 hours. The solvent was removed at reduced pressure and most of the excess benzyl alcohol was removed at 80°/1 mm. NaHCO3 solution was added and the product was extracted with ethyl acetate. The dried extract was concentrated at reduced pressure and the residue was purified by HPLC using 25% ethyl acetate-hexane to give 2.78 g (45% yield) of [3,5-bis[(1 -oxodecyl)amino]phenyl]carbamic acid phenylmethyl ester as a yellow foam. The nmr and mass spectra were compatible with the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446189
Source datasetuspto-grants-1995_08
ORD IDord-ca0625e1b6464aafa00f19c2be6f34a4
Source noteuspto-grants-1995_08