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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108746Generated: October 30, 2026

Sodium borohydride → HCID 22627373, compound

https://huagongshe.com/reaction/1108746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22627257HCID 22627257—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22627373HCID 2262737339.8%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 1-(2-chlorobenzyl)-3-isobutyryl-2-propylindole-6-carbonitrile (70 mg) in a mixture of methanol (2 ml) and tetrahydrofuran (2 ml) was added sodium borohydride (21 mg) at 25° C. After stirred at 25° C. for 2 hours, the reaction mixture was partitioned between ethyl acetate and 1N hydrochloric acid. The organic layer was washed with water and brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was crystallized from diisopropyl ether to give 1-(2-chlorobenzyl)-3-(1-hydroxy-2-methylpropyl)-2-propylindole-6-carbonitrile (28 mg) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069156
Source datasetuspto-grants-2000_05
ORD IDord-b18b8376ba9c43d28e0229070eccd91c
Source noteuspto-grants-2000_05