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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860637Generated: November 2, 2026

HCID 18624145, compound → HCID 18624173, compound

https://huagongshe.com/reaction/1860637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18624145HCID 18624145—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
SolventEthanolHCID 702—
ProductHCID 18624173HCID 1862417380%

Reaction Steps

The acid from STEP 3 (0.5 g) was suspended in absolute EtOH (3.0 mL), added 4N HCl/dioxane (2.0 mL) and stirred overnight at room temperature, and heated to reflux for 1 h. The solution was concentrated to dryness and the residue was dissolved in EtOAC (15 mL), washed with water, dried and concentrated to dryness. The resulting syrup (0.4 g) was dissolved in EtOH (10 mL), added acetic acid (0.1 mL), Pd/C (10%, 0.25 g), and stirred in an atmosphere of hydrogen gas at 50 psi at room temperature. After 16 h, the catalyst was removed by filtration, and the filtrate was concentrated to dryness under reduced pressure. The resulting colorless syrup was dried in vacuo to give the title compound (0.34 g, 80%): Rf=0.44 (50% EtOAc/Hexane); 1H -NMR (CDCl3) δ7.02 (d, 2H); 6.73 (d, 2H); 4.12 (q, 2H); 2.58 (s, 2H); 2.15 (d, 2H); 1.24 (t, 3H); 0.98 (s, 6H); ES-MS m/z 235(M-H); HRMS calcd C14H21O3 (MH+) 237.1485, found 237.1511.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531494B1
Source datasetuspto-grants-2003_03
ORD IDord-fb8de788e7c746ea9721fb3debbd7ecf
Source noteuspto-grants-2003_03