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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353506Generated: October 27, 2026

Diisobutylaluminumhydride → [1-(2-Trimethylsilanyl-ethanesulfonyl)-1H-indol-5-yl]-methanol

https://huagongshe.com/reaction/1353506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant1-(2-trimethylsilanylethanesulfonyl)-1H-indole-5-carboxylic acid ethyl esterHCID 25135864—
SolventTolueneHCID 1140—
Product[1-(2-Trimethylsilanyl-ethanesulfonyl)-1H-indol-5-yl]-methanolHCID 22596206—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of diisobutylaluminum hydride (82.9 mL, 1M in toluene, 82.9 mmol) was added slowly at 0° C. to the solution of 1-(2-trimethylsilanyl-ethanesulfonyl)-1H-indole-5-carboxylic acid ethyl ester (8.81 g, 25.9 mmol) in toluene (200 mL). After it was stirred at 0° C. for 45 min, the reaction was quenched by the addition of methanol (26 mL), pulverized sodium sulfate decahydrate (194 g) and celite (26 mL). The mixture was warmed up to room temperature in 1 h and filtered through a pad of celite. Solvents were removed in vacuo to afford the title compound as a very viscous liquid, which solidified upon cooling. A white solid (8.08 g, 100% yield). 1H-NMR (CDCl3, 500 MHz) δ 7.87 (d, J=8.5 Hz, 1H), 7.62 (s, 1H), 7.44 (d, J=3.7 Hz, 1H), 7.35 (dd, J=8.6, 1.5 Hz, 1H), 6.66 (d, J=3.7 Hz, 1H), 4.79 (s, 2H), 3.18–3.14 (m, 2H), 1.73 (s, 1H), 0.85–0.82 (m, 2H), −0.06 (s, 9H). Mass spec. 312.14 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220862B2
Source datasetuspto-grants-2007_05
ORD IDord-4abc715b96b84e39ae6d121a798769b0
Source noteuspto-grants-2007_05