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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494937Generated: October 30, 2026

Sodium Bicarbonate → HCID 57682927, compound

https://huagongshe.com/reaction/494937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
Reactant6-Hydroxy-3,4-dihydro-1(2H)-naphthalenoneHCID 4679494—
ReactantHCID 57682846HCID 57682846—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 57682927HCID 5768292782%

Reaction Steps

200 mg of 5-(2,3-dihydroxypropyl)-6-methoxy-1-tetralone synthesized from 6-hydroxy-1-tetralone according to the methods described in Example 7, (1)-(4), was dissolved in a mixed solution consisting of 5 ml of methanol and 3 ml of tetrahydrofuran. Thereafter, 401 mg of methoxylamine hydrochloride and 394 mg of sodium acetate were added to the reaction solution, and the obtained mixture was then stirred at room temperature. After completion of the reaction, a saturated sodium bicarbonate aqueous solution and ethyl acetate were added to the reaction solution, so as to separate an organic layer. The obtained organic layer was washed with a saturated sodium bicarbonate aqueous solution and a saturated sodium chloride solution, and then dried over anhydrous magnesium sulfate. After removing the drying agent by filtration, the organic layer was concentrated under a reduced pressure, so as to obtain 183 mg of 5-(2,3-dihydroxypropyl)-6-methoxy-3,4-dihydro-2H-naphthalen-1-one O-methyloxime. The subject compound was obtained from the thus obtained compound according to the method described in Example 1, (4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538123B2
Source datasetuspto-grants-2009_05
ORD IDord-e3e9651e51954128b427738ba0bceceb
Source noteuspto-grants-2009_05