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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306872Generated: November 1, 2026

2-Aminothiophenol → HCID 22629953, compound

https://huagongshe.com/reaction/2306872

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
ReactantPotassium CarbonateHCID 11430—
Reactant6-chloro-8-(chloromethyl)-4H-1,3-benzodioxineHCID 2776780—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 22629953HCID 22629953—

Reaction Steps

2-aminothiophenol (1.25 g, 10 mmol), 6-chloro-8-(chloromethyl)-4H-1,3-benzodioxine (2.17 g, 10 mmol) and potassium carbonate (4.10 g, 30 mmol) were combined in absolute ethanol (100 mL) and stirred 18 h. Dilute with ethyl acetate and wash with saturated sodium bicarbonate solution then brine. The solution was dried over sodium sulfate and the solvent removed in vacuo. The residue was dissolved in methanol and treated with MP BH4− resin (Argonaut 3.16 mmol/g) and potassium carbonate for 48 h. The mixture was filtered and the solvent removed in vacuo. The resulting oil was dissolved in dichloromethane and passed through a 5 g plug of silica gel. The solvent was removed in vacuo and the residue was precipitated from diethyl ether with a solution of hydrogen chloride in dioxane to give the product as an off white powder, 2.52 g (74%). MS (ESI+) for C15H14ClNO2S m/z 308 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06828446B2
Source datasetuspto-grants-2004_12
ORD IDord-56dfbcb2a8f545b8b8125273e12863b8
Source noteuspto-grants-2004_12