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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192969Generated: October 31, 2026

Hydrochloric Acid → Isoxazole, 3-[[(2,6-difluorophenyl)methyl]thio]-4,5-dihydro-5,5-dimethyl-

https://huagongshe.com/reaction/1192969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-Difluorobenzyl alcoholHCID 87921—
ReactantThioureaHCID 2723790—
Reactant3-Methylsulfonyl-5,5-dimethyl-2-isoxazolineHCID 12137656—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductIsoxazole, 3-[[(2,6-difluorophenyl)methyl]thio]-4,5-dihydro-5,5-dimethyl-HCID 1213765526%

Reaction Conditions

Temperature140 °C

Reaction Steps

2,6-Difluorobenzyl alcohol (0.2 ml, 1.8 mmol), thiourea (165 mg, 2.2 mmol), aqueous hydrochloric acid (2M) (2.7 ml) and 1,4-dioxane (3 ml) were mixed and the mixture heated in a sealed vessel in the microwave at 140° C. for 10 minutes. Potassium carbonate (1.1 g, 8 mmol) and 3-methanesulfonyl-5,5-dimethyl-4,5-dihydroisoxazole (380 mg, 2.1 mmol) were added and the mixture was stirred in an open vessel for 10 minutes. The mixture was heated in a sealed vessel in the microwave at 150° C. for 10 minutes. The mixture was diluted with water and extracted with ethyl acetate. The organic extract was washed with water, dried over magnesium sulfate and concentrated. The crude material was purified by chromatography on silica gel (eluent: ethyl acetate/hexane) to give the product as a white solid (120 mg, 26% yield). M.p. 85-87° C. 1H-NMR (400 MHz, CDCl3): 1.43 (6H, s, Me), 2.82 (2H, s, CH2), 4.36 (2H, s, CH2), 6.90 (2H, d, CH), 7.26 (1H, t, CH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680290B2
Source datasetuspto-grants-2014_03
ORD IDord-ad87b5f6862149629b235e233ef3f8d0
Source noteuspto-grants-2014_03