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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132727Generated: October 25, 2026

Pyridine → HCID 23125916, compound

https://huagongshe.com/reaction/132727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantTetrahydrofuranHCID 8028—
Reactant9H-Fluorene-9,9-dimethanolHCID 345022—
SolventWaterHCID 962—
ProductHCID 23125916HCID 2312591689%

Reaction Steps

To 11.3 g (0.05 mol) 9,9-dihydroxymethylfluorene was added 50 ml tetrahydrofuran, then added 12.1 ml (0.15 mol) pyridine with stirring. To the resulting homogenous mixture was slowly added 14.5 ml (0.125 mol) benzoyl chloride. The mixture was stirred at room temperature for 1 hour, and then heated refluxing for 4 hours. Upon reaction completion, 70 ml water was added to dissolve the resulting salt. The mixture was extracted with toluene. The organic phase was separated, washed with saturated saline for two times, dried over anhydrous sodium sulfate. The solvent was removed to give a white solid. Recrystallization from ethyl acetate gave 9,9-bis(benzoyloxymethyl)fluorene as a white crystal, the yield was 89%, and m.p. was 144-146° C. 1HNMR: δ (ppm) 4.74(s, 4H, CH2), 7.25-7.75(m, 18H, ArH)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388061B2
Source datasetuspto-grants-2008_06
ORD IDord-a7d2e366e4a44ea7acb857e3294796d8
Source noteuspto-grants-2008_06