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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393854Generated: November 3, 2026

Imidazole → 2-[4-(octyloxy)phenyl]-N-(3-thioxo-3H-1,2,4-dithiazol-5-yl)acetoamide

https://huagongshe.com/reaction/1393854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantSodium hydrideHCID 24758—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantXanthane hydrideHCID 2735329—
Reactant2-[4-(Octyloxy)phenyl]acetic acidHCID 12387351—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-[4-(octyloxy)phenyl]-N-(3-thioxo-3H-1,2,4-dithiazol-5-yl)acetoamideHCID 5968050521.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-[4-(Octyloxy)phenyl]acetic acid (0.900 g, 3.40 mmol) was dissolved in tetrahydrofuran (11 ml), and 1,1′-carbonyldiimidazole (0.622 g, 4.09 mmol) was added thereto. The imidazole mixture was stirred for 1 hour at 0° C. Sodium hydride (60% oil suspension 0.136 g, 3.40 mmol) was suspended in tetrahydrofuran (11 ml), and 3-amino-1,2,4-dithiazole-5-thione (0.511 g, 3.40 mmol) was added thereto. After being stirred for 30 minutes at 0° C., the reaction mixture, with the imidazole mixture added thereto, was stirred for 3 hours at 0° C. The mixture, with water added thereto, was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over MgSO4, and then concentrated. The obtained residue was purified by silica gel column chromatography (chloroform), to give 2-[4-(octyloxy)phenyl]-N-(3-thioxo-3H-1,2,4-dithiazol-5-yl)acetoamide (Compound 6) (0.290 g, 21%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348017B2
Source datasetuspto-grants-2008_03
ORD IDord-b5e92dda736a4f58a3e179df992b4852
Source noteuspto-grants-2008_03