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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757121Generated: November 1, 2026

Anisole → HCID 19973436, compound

https://huagongshe.com/reaction/1757121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 15290093HCID 15290093—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 19973436HCID 1997343667.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

6.15 g (12.4 mmol) of the 2-benzyloxy-1-((4-methoxybenzylthio)(methylimino)methyl)-1-(4-nitro-imidazol-1-yl)cyclohexane prepared in the Preparative Example 14 was dissolved in 25 ml of trifluoroacetic acid under cooling with ice, followed by the addition of 5 ml of anisole. The obtained mixture was stirred at 0° C. for 10 minutes to give a dark-brown solution, which was pored onto a mixture comprising a saturated aqueous solution of sodium hydrogencarbonate and ice. The obtained mixture was extracted with ethyl acetate. The organic phase was washed with a saturated aqueous solution of common salt, dried over anhydrous sodium sulfate, and concentrated in a vacuum. The residue (8.02 g) was purified by silica gel column chromatography [solvent: dichloromethane/acetone (40:1)], and recrystallized from dichloromethane/diisopropyl ether to give 3.14 g of the title compound as a colorless crystal (yield: 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05444066
Source datasetuspto-grants-1995_08
ORD IDord-81f9968b7f554cfba6347320e4d787b1
Source noteuspto-grants-1995_08