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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 84979Generated: October 27, 2026

Water → Triphenylsulfonium ((1-adamantyl)methoxycarbonyl)difluoromethanesulfonate

https://huagongshe.com/reaction/84979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriphenylsulfonium BromideHCID 11984010—
Reactant(Adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonic acid tert-butylammonium saltHCID 131731911—
SolventChloroformHCID 6212—
ProductTriphenylsulfonium ((1-adamantyl)methoxycarbonyl)difluoromethanesulfonateHCID 4422473292%

Reaction Steps

Within a 1-L three-neck flask, 122 g (purity: 99%, 307 mmol, 1.0 eq) of the (adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonic acid tert-butylammonium salt obtained in Example 5-b was dissolved in 500 g of chloroform. To the resulting solution, 400 g of water and 110.5 g (322 mmol, 1.05 eq) of triphenylsulfonium bromide were added. This reaction solution was stirred for 1 hour. After the reaction, the reaction solution was separated into an organic layer and an aqueous layer. The organic layer was washed with water, followed by distillating chloroform from the washed organic layer. The thus-obtained concentrated solution was dissolved in a mixed solvent of chloroform, ethyl acetate and diisopropyl ether and then recrystallized. With this, 166 g of target triphenylsulfonium (adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonate was obtained (yield: 92%, purity: 99%). No fluorine ion (F−) was detected from any liquid waste of this step. Further, 200 ppb of sodium ion (Na+) was detected from the triphenylsulfonium (adamantane-1-ylmethyl)oxycarbonyldifluoromethanesulfonate obtained in this step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846966B2
Source datasetuspto-grants-2014_09
ORD IDord-acfa2cd248d44fc8bd2cb4c3be34f306
Source noteuspto-grants-2014_09