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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826210Generated: November 1, 2026

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

https://huagongshe.com/reaction/1826210

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) was treated with aqueous potassium hydroxide (45%, 25.5 g, 204 mmol) with vigorous stirring, and the mixture was heated to 95° C. and stirred at this temperature for 18 hrs. The reaction was then cooled to ambient temperature and diluted with water (50 mL) and CH2Cl2 (100 mL), the layers were separated, and the organic phase was washed with water (50 mL) and saline (20 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was 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) were 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 numberUS07049443B2
Source datasetuspto-grants-2006_05
ORD IDord-bf2845d0d70945358396c41773006594
Source noteuspto-grants-2006_05