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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585308Generated: October 31, 2026

Pyrrolidine → HCID 22340335, compound

https://huagongshe.com/reaction/585308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactant6-Methoxy-2-naphthaldehydeHCID 76991—
ReactantSodiumHCID 5360545—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22340335HCID 22340335100.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 6-methoxy-2-naphthaldehyde (3.00 g, 16.1 mmol) and pyrrolidine (2.69 ml, 32.2 mmol) in tetrahydrofuran (32 ml) and acetic acid (16 ml) was added sodium triacetoxyhydroborate. (6.83 g, 32.2 mmol) at 0° C., and the mixture was stirred at room temperature for 7 hours. The solvent was distilled off under reduced pressure, 1N hydrochloric acid was added to the resulting oil, and the mixture was washed with diethyl ether. An 8N aqueous sodium hydroxide solution was added to the aqueous layer, followed by extraction with ethyl acetate. The extract was washed with an aqueous saturated sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was concentrated under reduced pressure to obtain the titled compound (3.89 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06930185B2
Source datasetuspto-grants-2005_08
ORD IDord-b9b67dd492b94c06a8ad8022cafe1ea4
Source noteuspto-grants-2005_08