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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844911Generated: November 1, 2026

Tetrahydrofuran → HCID 58409906, compound

https://huagongshe.com/reaction/1844911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantHCID 58409939HCID 58409939—
ProductHCID 58409906HCID 58409906—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

A solution of 2-(piperidin-1-yl)-4-p-tolyl-9H-fluorene-1-carbonitrile (364 mg) in THF was added sodium hydride (40 mg) and was stirred at 0-5° C. for less than five minutes. After completion, the reaction solvent was evaporated under vacuum and the crude solid obtained was quenched with ice water and subsequently neutralized by dilute HCl. The precipitate thus obtained was filtered and purified on a silica gel column using ethyl acetate-hexane as eluent. Red solid; mp 230-232° C.; ESMS 379 (M++1); IR (KBr) 1703 cm−1 (CO), 2219 (CN); 1H NMR (300 MHz, CDCl3) δ 1.60-1.64 (m, 2H, CH2), 1.79-1.84 (m, 4H, 2CH2), 2.48 (s, 3H, CH3), 3.19-3.24 (m, 4H, 2CH2), 6.65-6.70 (m, 1H, ArH), 6.87 (s, 1H, ArH), 7.14-7.19 (m, 2H, ArH), 7.28-7.33 (m, 4H, ArH), 7.63-7.67 (m, 1H, ArH). HRMS calcd. for C26H22N2O 378.1732 found 378.1728.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946682B2
Source datasetuspto-grants-2015_02
ORD IDord-aec5117bed7549ed8307fc18a64b9786
Source noteuspto-grants-2015_02