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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268674Generated: October 30, 2026

Lithium borohydride → HCID 12272805, compound

https://huagongshe.com/reaction/268674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantEthyl 7-(1-methylethyl)-α-oxo-1H-indole-3-acetateHCID 12272804—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12272805HCID 12272805—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446122B2
Source datasetuspto-grants-2008_11
ORD IDord-e8bda693b9704b21a2dde45d77a26463
Source noteuspto-grants-2008_11