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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33415Generated: October 25, 2026

Water → Tropenol 9-fluorofluorene-9-carboxylate

https://huagongshe.com/reaction/33415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
Reactant(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 2734690—
ReactantTropenol 9-hydroxyfluorene-9-carboxylateHCID 86593872—
SolventDichloromethaneHCID 6344—
ProductTropenol 9-fluorofluorene-9-carboxylateHCID 86593873—

Reaction Steps

1.66 mL (0.009 mol) of bis-(2-methoxyethyl)aminosulfur trifluoride are placed in 10 mL dichloromethane and within 20 minutes at 15°-20° C., a solution of 2.4 g (0.007 mol) of 4a in 25 mL dichloromethane is added dropwise thereto. The mixture is stirred for 20 hours at ambient temperature, cooled to 0° C., and carefully combined with 80 mL of water with thorough stirring. Then the mixture is carefully adjusted to pH 8 with aqueous NaHCO3 solution, the organic phase is separated off, the aqueous phase is extracted again with dichloromethane, the combined organic phases are washed with water, dried over magnesium sulfate, and evaporated to dryness. The hydrochloride is precipitated and recrystallized from acetonitrile-diethyl ether. Then the free base is liberated again using 10% aqueous sodium carbonate solution. Yield: 1.05 g bright yellow crystals (53% of theoretical yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429600B2
Source datasetuspto-grants-2008_09
ORD IDord-3b0cf7fbe1d142a6b74aa89d3a600a16
Source noteuspto-grants-2008_09