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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863521Generated: October 27, 2026

Acetic Acid → 1-Acetamido-7-pyrrolidin-1-yl-5,6,7,8-tetrahydronaphthalene

https://huagongshe.com/reaction/863521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPyrrolidineHCID 31268—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant8-Acetamido-2-tetraloneHCID 13424111—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventBenzene dimethylformamideHCID 19608675—
Product1-Acetamido-7-pyrrolidin-1-yl-5,6,7,8-tetrahydronaphthaleneHCID 1969624669.7%

Reaction Steps

A mixture of 8-acetamido-2-tetralone (0.4 g, 2 mmol), pyrrolidine (0.28 g, 4 mmol) and tosic acid (10 mg) in benzene:DMF (5:1, 12 mL) was heated at reflux with a Dean-Stark trap for 4 h. The solvent was evaporated and the residue dissolved in 1:1 MeOH:THF (10 mL). Acetic acid (1 mL) and sodium cyanoborohydride (0.25 g, 4 mmol) were added, and the reaction stirred for 16 h. The solvent was evaporated and the residue taken up in water:methylene chloride. The aqueous layer was basified with 12.5% NaOH, and back extracted. The combined organic phase was dried over sodium sulfate, filtered and evaporated. The residue solidified upon standing, and was crystallized from tolune:hexane to give the product (0.36 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05721234
Source datasetuspto-grants-1998_02
ORD IDord-fa30521bf41b4b8b86dac3d46a1e75a9
Source noteuspto-grants-1998_02