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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908537Generated: October 27, 2026

Lithium borohydride → HCID 59129177, compound

https://huagongshe.com/reaction/1908537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 16752708HCID 16752708—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59129177HCID 5912917773.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

Ethyl 5-(1-(benzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)-1H-indole-2-carboxylate (1.18 g, 3.0 mmol) was added to a solution of LiBH4 (132 mg, 6.0 mmol) in THF (10 mL) and water (0.1 mL). The mixture was allowed to stir for 16 h at 25° C. before it was quenched with water (10 mL) and slowly made acidic by addition of 1 N HCl. The mixture was extracted with three 50-mL portions of ethyl acetate. The organic extracts were dried over Na2SO4 and evaporated to yield 1-(benzo[d][1,3]dioxol-5-yl)-N-(2-(hydroxymethyl)-1H-indol-5-yl)cyclopropanecarboxamide (770 mg, 73%). A small amount was further purified by reverse phase HPLC. ESI-MS m/z calc. 350.4. found 351.3 (M+1)+; retention time 2.59 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598181B2
Source datasetuspto-grants-2013_12
ORD IDord-11979664bbfc4c3da0f13e6898ad8a7c
Source noteuspto-grants-2013_12