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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075475Generated: October 24, 2026

Methyl (5-fluoro-2-methyl-1H-inden-3-yl)acetate → 5-fluoro-2-methyl-1H-3-indenyl-(2-hydroxy) ethane

https://huagongshe.com/en/reaction/1075475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl (5-fluoro-2-methyl-1H-inden-3-yl)acetateHCID 15434585—
SolventTetrahydrofuranHCID 8028—
Product5-fluoro-2-methyl-1H-3-indenyl-(2-hydroxy) ethaneHCID 1393329363%

Reaction Steps

To a solution of methyl 5-fluoro-2-methyl-3-indenyl- acetate (24 g) in dry THF (300 ml) lithiumaluminum hydride (6.9 g) is added. The mixture is stirred at room temperature for 1.5 hours. Excess LiA1H4 is destroyed with saturated aqueous NaHSO4 solution. The organic phase is concentrated in vacuo, and the crude product is purified via silica gel column chromatography elution with methylene chloride. The residue is recrystallized from hexane to give 5-fluoro-2-methyl-1H-3-indenyl-(2-hydroxy) ethane (yield 63%; m.p. 65-66.5° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05902827
Source datasetuspto-grants-1999_05
ORD IDord-d86fab6ae11c445a8ae1cf5d99ddf104
Source noteuspto-grants-1999_05