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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723841Generated: October 30, 2026

Potassium Hydroxide → 3-fluoro-4-(tetrahydro-2H-thiopyran-4-yl)benzenamine

https://huagongshe.com/reaction/723841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant2-methylpropyl[3-fluoro-4-(tetrahydro-2H-thiopyran-4-yl)phenyl]carbamateHCID 15550046—
SolventEthylene GlycolHCID 174—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-fluoro-4-(tetrahydro-2H-thiopyran-4-yl)benzenamineHCID 21877658—

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 2-methylpropyl[3-fluoro-4-(tetrahydro-2H-thiopyran-4-yl)phenyl]carbamate (Step 1, 2.12 g, 6.81 mmol) in ethylene glycol (25 mL) is treated with aqueous potassium hydroxide (45%, 25.5 g, 204 mmol) with vigorous stirring, and the mixture is heated to 95° C. and stirred at this temperature for 18 h. The reaction is then cooled to ambient temperature and diluted with water (50 mL) and CH2Cl2 (100 mL), the layers are separated, and the organic phase is washed with water (50 mL) and saline (20 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product is chromatographed on a Flash 40M 90 g silica gel cartridge with a gradient of EtOAc/heptane (15/85–25/75), and those fractions with an Rf=0.32 by TLC (EtOAc/hexanes, 25/75) are pooled and concentrated to give the title compound, mp 96–98° C.; MS (ESI+) for C11H14NFS m/z 212 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141588B2
Source datasetuspto-grants-2006_11
ORD IDord-631935d25b134806aae40d6afe4a8e9e
Source noteuspto-grants-2006_11