HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177678Generated: October 26, 2026
Diisobutylaluminumhydride → [1-(2-Trimethylsilanyl-ethanesulfonyl)-1H-indol-5-yl]-methanol
https://huagongshe.com/reaction/1177678
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | 1-(2-trimethylsilanylethanesulfonyl)-1H-indole-5-carboxylic acid ethyl ester | HCID 25135864 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | [1-(2-Trimethylsilanyl-ethanesulfonyl)-1H-indol-5-yl]-methanol | HCID 22596206 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842808B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-6e3ad7e806444e8d811281a05c6f2bf8 |
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| Source note | uspto-grants-2010_11 |
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