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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850069Generated: November 1, 2026

Triethylamine → HCID 68294609, compound

https://huagongshe.com/reaction/1850069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1H-Indole-6-carboxaldehydeHCID 2773435—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 68294015HCID 68294015—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofurane dichloromethaneHCID 21919333—
ProductHCID 68294609HCID 68294609112%

Reaction Steps

A solution of the hydrochloride salt of methyl 4-(azetidin-3-ylidenemethyl)-3-chlorobenzoate (0.20 g, 0.73 mmol) in THF:DCM (2:1) (25 mL) was neutralized by addition of triethylamine (0.14 mL, 0.88 mmol). After stirring at room temperature for 20 mins, indole-6-carboxaldehyde (0.16 g, 1.00 mmol) and sodium triacetoxyborohydride (0.50 g, 2.37 mmol) were added and the reaction mixture was heated at 50° C. overnight. It was then diluted with DCM (50 mL) and washed with saturated sodium bicarbonate (3×25 mL) and brine (1×15 mL). The organic layer was separated, dried (Na2SO4) and filtered. The filtrate was concentrated under vacuum to give the crude product which was purified by silica gel column chromatography using 10-40% EtOAc in hexanes as eluent. Fractions containing the pure product were pooled and evaporated to give 0.3 g of methyl 4-((1-((1H-indol-6-yl)methyl)azetidin-3-ylidene)methyl)-3-chlorobenzoate (0.30 g) as a colorless oil. ES+(M+H)+367

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957066B2
Source datasetuspto-grants-2015_02
ORD IDord-e03e205ef80549e7a4d0d560ee1206bc
Source noteuspto-grants-2015_02