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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722435Generated: October 30, 2026

Tetrahydrofuran → HCID 58742335, compound

https://huagongshe.com/reaction/722435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 68831343HCID 68831343—
ProductHCID 58742335HCID 5874233513%

Reaction Steps

A solution of (2R,4aR,10aR)-7-(tert-butyidimethylsilanyloxy)-4a-ethyl-2-hydroxy-2-pyridin-4-yl-1,4,4a,9,10,10a-hexahydro-2H-phenanthren-3-one (32 mg, 0.65 mmol) in tetrahydrofuran (5 mL) was cooled to −78° C. and treated with a 1.0 M solution of methyllithium/lithium iodide complex in tetrahydrofuran (0.65 mL, 0.65 mmol). The mixture was allowed to stir from −78° C. to room temperature over 3 days and was then quenched with saturated aqueous ammonium chloride solution and water. The mixture was extracted four times with ethyl acetate. The combined extracts were washed with brine, dried over sodium sulfate and concentrated to a solid that was triturated with hexane and diethyl ether. The title compound (3 mg, 13%) was isolated from the solid by chromatography on silica gel eluting with a gradient of 50% ethyl acetate in hexane to 100% ethyl acetate. Mass spectrum (m/e) 354 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138406B2
Source datasetuspto-grants-2006_11
ORD IDord-219465532822484a807fbdbf4a5a7bca
Source noteuspto-grants-2006_11