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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943571Generated: October 25, 2026

Triethylamine → Bis(4-tert-butylphenyl)iodonium 2-(adamantane-1-carbonyloxy)ethanesulfonate

https://huagongshe.com/reaction/1943571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Adamantanecarbonyl chlorideHCID 98915—
ReactantSodium IsethionateHCID 517063—
ReactantBis(4-tert-butylphenyl)iodanium hydrogen sulfateHCID 20205689—
CatalystBenzyltrimethylammonium chlorideHCID 5963—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductBis(4-tert-butylphenyl)iodonium 2-(adamantane-1-carbonyloxy)ethanesulfonateHCID 8664223995%

Reaction Steps

In water, 5.1 g (0.035 mole) of sodium isethionate and 6.4 g (0.053 mole) of benzyltrimethylammonium chloride were mixed and dissolved. The solution was concentrated by removing water in vacuum. The concentrate was dispersed in 55 g of acetonitrile. To the dispersion, 5.2 g (0.052 mole) of triethylamine and 0.42 g (0.0035 mole) of 4-(dimethylamino)pyridine were added, and under ice cooling, 20.6 g (0.052 mole) of 50% adamantane-1-carbonyl chloride in dichloromethane was then added dropwise. The reaction mixture was stirred at room temperature over night. Water was added to quench the reaction, from which acetonitrile was distilled off in vacuum. An amount (0.0088 mole) of bis(4-tert-butylphenyl)iodonium hydrogensulfate prepared in Synthesis Example 1-6 and 50 g of methyl isobutyl ketone were added to the residue, followed by stirring at room temperature for 1 hour. The organic layer was taken out, washed with water, and concentrated in vacuum. Diisopropyl ether was added to the concentrate for recrystallization. The crystals were collected and dried, obtaining the target compound, bis(4-tert-butylphenyl)iodonium 2-(adamantane-1-carbonyloxy)ethanesulfonate. White crystals, 5.7 g, yield 95%. The compound, designated PAG-6, has the following structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394570B2
Source datasetuspto-grants-2013_03
ORD IDord-f071d8395b884546968fc8bf3741de5f
Source noteuspto-grants-2013_03