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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460337Generated: October 27, 2026

Hydrazine → HCID 178486505, compound

https://huagongshe.com/reaction/460337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
Reactant5,6-Dimethoxy-1-indanoneHCID 75018—
Reactant3,5-Dichlorophenyl isothiocyanateHCID 138776—
ReactantLithium hexamethyldisilaneHCID 57425481—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178486505HCID 178486505—

Reaction Steps

A mixture of 5,6-dimethoxyindan-1-one, Compound 3a, (4 g, 0.021 mole), 3,5-dichlorophenyl isothiocyanate, Compound 3b, (4.45 g, 0.022 mole) and THF (30 mL) was added to lithium hexamethyldisilane (26.9 mL, 0.269 mole) dropwise at room temperature with stirring. Hydrazine (1.04 mL, 0.032 mole) and acetic acid (1.65 mL) were added to the reaction mixture, which was then stirred at room temperature for 12 hrs. The reaction continued at 75° C. overnight. The resulting organics were first diluted with ethyl acetate (100 mL), then washed with water and brine solution, dried (Na2SO4), and solvent was removed in vacuo. The chemical residues were recrystallized from ethanol. The first and second crops of solid were combined and dissolved in hot CH3CN, to which an equal volume of HCl-ether solution was added to precipitate the title compound (Compound 19), which was collected and dried under vacuum at 60° C. mp>270° C.; MS m/z 376 and 378 (M+H)+; 1HNMR (DMSO-d6): 3.44(s, 2H), 3.83(s, 3H), 3.82(s, 3H),6.93(s, 1H),7.19 (s, 1H), 7.21(s, 1H), 7.35(s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196110B2
Source datasetuspto-grants-2007_03
ORD IDord-98d9cb999b3f4aba9250b7907b37240f
Source noteuspto-grants-2007_03