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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725367Generated: October 30, 2026

Acetic Acid → HCID 22556753, compound

https://huagongshe.com/reaction/1725367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAllylamineHCID 7853—
ReactantIndole-7-carboxaldehydeHCID 2734629—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
ProductHCID 22556753HCID 2255675382%

Reaction Conditions

Temperature22 °C

Reaction Steps

Add allylamine (2.50 mL, 33.1 mmol), acetic acid (3.4 mL), and sodium triacetoxyborohydride (5.85 g, 27.6 mmol) to a solution of indole-7-carboxaldehyde (4.00 g, 27.6 mmol) in 1,2-dichloroethane (120 mL) at 20-24° C. and stir the resulting mixture at 20-24° C. for 5 hours. Add an additional 1.5 g (7.1 mmol) of sodium triacetoxyborohydride and stir the resulting mixture overnight. Dilute the mixture with dichloromethane (300 mL), wash carefully with aqueous sodium bicarbonate (100 mL), and separate the layers. Wash the organic layer sequentially with water (100 mL) and saturated aqueous sodium chloride (100 mL), dry over sodium sulfate, filter, and concentrate under reduced pressure. Subject the residue to silica gel chromatography, eluting with 10-30% ethyl acetate in hexanes. Combine fractions containing product and concentrate them under reduced pressure to provide the desired compound as a light yellow oil (4.21 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491716B2
Source datasetuspto-grants-2009_02
ORD IDord-646a4daa280849f0a35c17630bb371f0
Source noteuspto-grants-2009_02