HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268674Generated: October 30, 2026
Lithium borohydride → HCID 12272805, compound
https://huagongshe.com/reaction/268674
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Ethyl 7-(1-methylethyl)-α-oxo-1H-indole-3-acetate | HCID 12272804 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12272805 | HCID 12272805 | — |
Reaction Steps
To a solution of (7-isopropyl-1H-indol-3-yl)-oxo-acetic acid ethyl ester (0.97 g. 3.7 mmol) in tetrahydrofuran was added 2.0 M solution of lithium borohydride in tetrahydrofuran. The mixture was heated at 90° C. for 5 hours. It was quenched with 5% HCl, followed by saturated sodium bicarbonate. It was extracted with ethyl acetate. The extracts were dried over magnesium sulfate and evaporated to dryness to provide a crude 2-(7-isopropyl-1H-indol-3-yl)-ethanol. ESI (+) MS m/e=204 (MH+), ESI (−) MS m/e=202 (MH−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07446122B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-e8bda693b9704b21a2dde45d77a26463 |
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| Source note | uspto-grants-2008_11 |
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