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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527244Generated: November 4, 2026

Sodium hydride → HCID 71009605, compound

https://huagongshe.com/reaction/1527244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantTriisopropylsilyl chlorideHCID 139400—
Reactant(1H-indol-5-yl)methanolHCID 2773458—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71009605HCID 71009605—

Reaction Steps

To a solution of (1H-indol-5-yl)-methanol (1.00 g, 6.79 mmol) in THF (60 mL), cooled to 0° C., was added sodium hydride (60% in mineral oil; 1.36 g, 34.0 mmol) portionwise. After stirring for 5 min, triisopropylsilyl chloride (2.88 mL, 13.6 mmol) was added, and the resulting solution was stirred at RT for 2 h. The reaction was quenched by addition of a saturated aqueous NaHCO3 solution at 0° C. The aqueous layer was repeatedly extracted with EtOAc, and the combined organics were washed with H2O (1×) and brine (1×), dried (phase separator) and concentrated in vacuo. Purification by flash column chromatography on silica gel (eluent gradient: c-hexane to c-hexane/EtOAc 9:1) afforded the title compound as a white solid. TLC, Rf (c-hexane/EtOAc 9:1)=0.72. 1H-NMR (400 MHz, DMSO-d6): 5 ppm 7.61 (s, 1H), 7.49 (d, 1H), 7.32 (d, 1H), 6.93 (d, 1H), 6.57 (d, 1H), 4.92 (s, 2H), 1.60-1.85 (m, 3H), 1.01-1.12 (m, 39H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085555B2
Source datasetuspto-grants-2015_07
ORD IDord-c1a27ed24bd441c8a96272ab9f1678ed
Source noteuspto-grants-2015_07