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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471863Generated: October 30, 2026

Methyl iodide → HCID 178503593, compound

https://huagongshe.com/reaction/1471863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
Reactant2-PhenylacetophenoneHCID 9948—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 178418922HCID 178418922—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178503593HCID 178503593—

Reaction Steps

To a solution of 1,2-diphenylethanone (5 g, 25.5 mmol) in anhydrous THF (10 mL) was added a solution of 1.0 M KO-t-Bu in THF (108 mL). The reaction was stirred for 15 min at room temperature, then CS2 (2.09 g, 27.5 mmol) was added. After 10 min, iodomethane (7.96 g, 56.1 mmol) was added and the reaction was stirred for 4 h. The reaction was washed with saturated NaHCO3 solution and dried over MgSO4. The filtrate was concentrated under reduced pressure and the residue was triturated with 10% ethyl acetate. The solid was suspended in ethanol and hydrazine hydrate (5.10 g, 102 mmol) was added at room temperature. The reaction was refluxed for 4 h. The reaction mixture was concentrated under reduced pressure and the residue was triturated with ethyl acetate/hexane to give the title compound as a white solid (5.2 g). LCMS m/z=267.27 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012478B2
Source datasetuspto-grants-2015_04
ORD IDord-8508d962a53940438517fa0d0d1c6cc7
Source noteuspto-grants-2015_04