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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379350Generated: October 30, 2026

Ethyl Acetate → HCID 21698569, compound

https://huagongshe.com/reaction/379350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHCID 21698574HCID 21698574—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
ProductHCID 21698569HCID 21698569—

Reaction Steps

To a solution of N-(3-ethyl-3,5,5-trimethylcyclohexyl)-2-hydroxy-3-nitrobenzamide (3.60 g) in ethyl acetate (75 ml) was added 5% Pd/C (0.40 g) catalyst. The resulting mixture was subjected to a hydrogen atmosphere (initial H2 pressure=50 psi) using a Parr shaker apparatus. When hydrogen uptake ceased (approximately 30 minutes), the hydrogen atmosphere was purged. A stir bar was added to the reaction bottle and to the stirred reaction mixture acetic-formic anhydride (3 ml) was added all at once. After stirring at room temperature for 30 minutes, the reaction was filtered, washed with saturated sodium bicarbonate solution (100 ml). then with a saturated sodium chloride solution (100 ml), dried (MgSO4) and the solvent evaporated to give the desired product as a white solid foam (3.5 g). An analytical sample could be prepared by recrystallization from a methanol/water mixture to give an off-white crystalline solid (m.p.=166-168° C.). 13C NMR (CDCl3) showed this material to be approximately a 6:4 mixture of diastereomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297401B1
Source datasetuspto-grants-2001_10
ORD IDord-81b8de6077244d4bbfa485f9dfc5e9ae
Source noteuspto-grants-2001_10