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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490230Generated: October 29, 2026

Ethanethiol → HCID 21480631, compound

https://huagongshe.com/reaction/1490230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantSodium hydrideHCID 24758—
ReactantSodiumHCID 5360545—
ReactantHCID 12016072HCID 12016072—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21480631HCID 2148063190.4%

Reaction Steps

To a solution of the 1-(9,10-dihydro-9,10-methanoanthracen-9-ylmethyl)-4-(2-fluoro-3-pyridyl)piperidin-4-ol (described in e. above) (2.00 g, 5.00 mmol, 1 eq) in THF (50 mL) under nitrogen was added the sodium salt of ethanethiol (0.90 g, 10.7 mmol, 2.2 eq). The thiolate salt was prepared from ethanethiol and sodium hydride under standard conditions. The reaction was heated to reflux for 18 h and quenched by pouring into water (100 mL). The aqueous phase was extracted with diethyl ether (2×100 mL), dried over anhydrous sodium sulfate, filtered, and reduced to an oil. The reaction product was purified by flash chromatography over silica gel (200 mL, eluent: 50% ether in hexane) to yield 2.00 g (90%) of the title compound. TLC analysis (Rf 0.29, 50% ether in hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05681840
Source datasetuspto-grants-1997_10
ORD IDord-6a1b7d27973e4a13a34b2133cedb68b2
Source noteuspto-grants-1997_10