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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703704Generated: October 30, 2026

Triethylamine → HCID 23501331, compound

https://huagongshe.com/reaction/703704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAdamantanoneHCID 64151—
ReactantBenzoic acid, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, methyl esterHCID 11715937—
CatalystZincHCID 23994—
Catalysttitanium(III) trichlorideHCID 10313229—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 23501331HCID 2350133182.2%

Reaction Steps

To a four-necked round-bottom flask equipped with a refluxing condenser and mechanical stirrer was added 1.5 L of dry THF under argon. Titanium trichloride (TiCl3, 200 g, 1.29 mol) was then added to the flask with stirring. After 15 minutes of stirring, powdered zinc (130 g, 2.0 mol) was added in portions and the flask was heated in hot water for 25 minutes. The reaction flask was then cooled in an ice-salt bath and the temperature of the mixture maintained at 5° to 7° C. Triethylamine (2.0 mL) was added to the suspension with caution (the reaction is extremely exothermic). The reaction started in approximately 5 to 10 minutes. After the reaction subsided, an additional amount of triethylamine (200 mL) was added and the mixture heated under reflux for 3 hours. After this period, a solution of methyl 3-tert-butyldimethylsiloxybenzoate (100 g, 0.37 mol) and 2-adamantanone (85.0 g, 0.57 mol) in 400 mL of dry THF was added dropwise to the refluxing mixture over 5 hours. The reaction mixture was then cooled to room temperature and was diluted with hexane (4 L) and the stirring continued. The suspended solids were then allowed to settle and the organic layer decanted. The black solid was washed with diethyl ether (2×1 L). Hexane (1 L) was added to the black material, followed by 1 L of water and the organic layer was removed. The aqueous layer was washed a second time with 1.5 L of hexane. The combined hexane and ether layers were then gravity filtered and the resulting solution was dried over anhydrous magnesium sulfate. Evaporation of the solvent under reduced pressure and chromatography over silica gel with 5% ethyl acetate/hexane gave 117 g (81% yield) of 2 as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04983779
Source datasetuspto-grants-1991_01
ORD IDord-9dcce1f30b2d4f7e9c03dd41fa9ccbbe
Source noteuspto-grants-1991_01