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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259822Generated: October 25, 2026

Diisobutylaluminum hydride → (1H-indol-2-yl)methanol

https://huagongshe.com/reaction/259822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantEthyl indole-2-carboxylateHCID 73125—
ReactantAcetone cardiceHCID 18522661—
SolventTetrahydrofuranHCID 8028—
Product(1H-indol-2-yl)methanolHCID 98783—

Reaction Conditions

Temperature-78 °C

Reaction Steps

In a 50-mL round-bottom flask, a total of 2.28 g (12 mmol) of ethyl 2-indolecarboxylate was dissolved in 15 mL of dry THF under N2. The solution was cooled to -78° C. (acetone-dry ice bath) and 24 mL (24 mmol) of 1.0M DIBAL in THF was added over a period of 1 h. The mixture was stirred for 2 h at -78° C., quenched with 10 mL of 1N HCl, then allowed to warm to room temperature. The reaction mixture was then extracted with ether (4×100 mL) and the ether layer was washed with 1N HCL (2×100 mL), dried over MgSO4, filtered, and evaporated in vacuo. The product was purified by flash chromatography (1:1 ethyl acetate:petroleum ether). Yield: 1.76 g (99%). 1H NMR (CDCl3): δ1.86 (t, 1H, J=6, OH), 4.82 (d, 2H, J=6), 6.40 (s, 1H), 7.0-7.3 (m, 2H), 7.34 (d, 1H, J=7.8), 7.58 (d, 1H, J=7.8), 8.36 (br s, 1H) MS (EI): m/z 147 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05523411
Source datasetuspto-grants-1996_06
ORD IDord-96f895a183034b818cda1ce120478271
Source noteuspto-grants-1996_06