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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63582Generated: October 25, 2026

Acetic Acid → 2-[(1H-Indol-7-ylmethyl)amino]-ethan-1-ol

https://huagongshe.com/reaction/63582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetaldehyde ammoniaHCID 522583—
ReactantIndole-7-carboxaldehydeHCID 2734629—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
Product2-[(1H-Indol-7-ylmethyl)amino]-ethan-1-olHCID 21950050—

Reaction Steps

To a solution of 7-formyl indole (2.4 g, 16.6 mmol) in 1,2-dichloroethane (60 mL) was added aminoethanol (1.2 mL, 19.8 mmol) followed by glacial acetic acid (2.0 mL) and sodium triacetoxyborohydride (3.5 g, 16.6 mmol). The reaction mixture was allowed to stir at room temperature for 16 hours. The reaction mixture was quenched by addition of water (10 mL) and 1.0 M sodium hydroxide (10 mL). The organic layer was then separated and the aqueous layer extracted with 1,2-dichloroethane (40 mL). The combined organic extracts were washed with saturated sodium bicarbonate (2×30 mL), water (2×50 mL), dried over anhydrous sodium sulfate and evaporated to dryness. 2-[(1H-indol-7-ylmethyl)-amino]-ethanol (4.4 g) was obtained as an oil LCMS (M+H)=189.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447088B2
Source datasetuspto-grants-2016_09
ORD IDord-6d082143eacc4623b3cf5fbe2eb69011
Source noteuspto-grants-2016_09