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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257826Generated: November 3, 2026

Water → 2-Acetamido-8-methoxytetralin

https://huagongshe.com/reaction/2257826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium AcetateHCID 517165—
Reactant8-Methoxy-2-tetraloneHCID 4136021—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
Product2-Acetamido-8-methoxytetralinHCID 3018920126.4%

Reaction Steps

To a solution of 5.18 gm of 8-methoxy-2-tetralone [described in J. Chem. Soc. 2636 (1965)] dissolved in 100 ml of methanol, were added 560 mg of sodium cyanoborohydride and 4.86 gm of ammonium acetate, and the mixture was stirred for 89 hours at room temperature. The reaction mixture was ice-cooled and adjusted to below pH 1, followed by the addition of 500 ml of water. After washing with ether, the water layer was adjusted to greater than pH 10 with potassium hydroxide and extracted with ether. The extract was dried over anhydrous magnesium sulfate, and the residue obtained by removing the solvent was dissolved in 50 ml of methylene chloride. 2 ml of pyridine and 2.4 ml of acetic anhydride were added to the solution, followed by stirring at room temparature for 1 hour. The reaction mixture was washed with 10% aqueous solution of hydrochloric acid, saturated aqueous solution of sodeum bicarbonate, and saturated brine in this order, and dried over anhydrous magnesium sulfate. After removal of the solvent, the residue was ctystallized in ethyl acetate and hexane to produce 2.47 gm of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05658920
Source datasetuspto-grants-1997_08
ORD IDord-f0c527cb6ffb45c28b4230b0c3beeaff
Source noteuspto-grants-1997_08