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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487940Generated: October 25, 2026

Acetic Acid → HCID 14181063, compound

https://huagongshe.com/reaction/487940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant8-Methoxy-2-tetraloneHCID 4136021—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN-(2-aminoethyl)ethylcarbamateHCID 21616286—
ProductHCID 14181063HCID 1418106346.2%

Reaction Steps

10.0 g (159 mmol) of sodium cyanoborohydride were added to the solution of 7.00 g (40 mmol) of 8-methoxy-2-tetralone, 8.00 g (61 mmol) of N-(2-aminoethyl)ethylcarbamate and 9.60 g (160 mmol) of glacial acetic acid at 0° C. After 15 hours at room temperature, the mixture was concentrated, taken up in tert.-butyl methyl ether, and treated with water. The pH of the aqueous phase was adjusted to 10 using sodium hydroxide solution. The mixture was stirred vigorously for 30 minutes. The organic phase was separated off, and the aqueous phase was extracted thoroughly with the last-mentioned solvent. Drying the organic phase and concentrating supplied an oil, which was purified by chromatography on silica gel (toluene/ethanol gradients with addition of 0.3% triethylamine). 5.40 g (46%) of the pure title compound were obtained as a brownish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298513
Source datasetuspto-grants-1994_03
ORD IDord-be45c86f17fc4dfca4f70bb9d4e00dfe
Source noteuspto-grants-1994_03