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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218337Generated: October 30, 2026

Hydroxyamine hydrochloride → 8-(1-Hydroxyiminoethyl)-10,11-dihydrodibenzo[b,f]thiepin-1,3-diol

https://huagongshe.com/reaction/2218337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
Reactant8-Acetyl-10,11-dihydrodibenzo[b,f]thiepin-1,3-diolHCID 15512543—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product8-(1-Hydroxyiminoethyl)-10,11-dihydrodibenzo[b,f]thiepin-1,3-diolHCID 7264085963.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

In ethanol, 180 mg of 8-acetyl-10,11-dihydrodibenzo[b,f]thiepin-1,3-diol (63) was dissolved, and an aqueous solution of 49 mg of hydroxylamine hydrochloride and 100 mg of sodium acetate dissolved in 1 mL of water was added thereto. The mixed solution was stirred at 120° C. for 3 hours, concentrated under reduced pressure and then, extracted with ethyl acetate. The organic layer was washed with water and a saturated sodium chloride solution and then, dried with anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent; hexane:ethyl acetate=1:1). Upon recrystallization from chloroform-hexane, 120 mg of skin-colored amorphous title compound was obtained (yield 63%). Melting Point: 215.4 to 217.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410997B2
Source datasetuspto-grants-2008_08
ORD IDord-f08d0aa20e944ba7bb40ad565bf91dcb
Source noteuspto-grants-2008_08