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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921032Generated: October 25, 2026

Sodium borohydride → [(1,2-dimethyl-1H-indol-3-yl)methyl](methyl)amine

https://huagongshe.com/reaction/1921032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1,2-Dimethyl-3-(methyliminomethyl)-1H-indoleHCID 14142219—
SolventEthanolHCID 702—
Product[(1,2-dimethyl-1H-indol-3-yl)methyl](methyl)amineHCID 1087790768%

Reaction Steps

1,2-Dimethyl-3-(methyliminomethyl)-1H-indole was taken up in ethanol (200 mL) and NaBH4 (2.6 g, 68.7 mmole) was added portionwise with stirring at RT (vigorous gas evolution). After 16 h the reaction was concentrated under vacuum, and the residue was basified with aqueous 1.0 N NaOH (200 mL). The mixture was extracted with Et2O (250 mL), and the combined Et2O extracts were washed with brine, dried (Na2SO4) and concentrated. Purification by flash chromatography on silica gel (5-10% (5% NH4OH/MeOH)/CHCl3) gave the title compound (8.47 g, 68%) as an oil which solidified in the freezer 1H NMR (400 MHz, CDCl3) δ 7.60 (d, J=7.7 Hz, 1H), 7.29 (d, J=8.0 Hz, 1H), 7.19 (t, 1H), 7.12 (t, 1H), 3.93 (s, 2H), 3.69 (s, 3H), 2.49 (s, 3H), 2.45 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173646B2
Source datasetuspto-grants-2012_05
ORD IDord-e52bb8a518db433b902508738edab3ad
Source noteuspto-grants-2012_05