Hydrochloric Acid → Methyl (4-ethoxy-3-fluorophenyl)carbamodithioate

Carbon disulfide (2.0 g, 26 mmol) was added to a mixture of 4-ethoxy-3-fluoroaniline (2.7 g, 17 mmol) and triethylamine (4.0 g, 40 mmol) while stirring. The mixture was stirred at room temperature for 10 hours, N,N-dimethylformamide (30 ml) was added thereto and methyl iodide (2.2 g, 16 mmol) was added dropwise. The mixture was stirred at room temperature for 30 minutes and dilute hydrochloric acid was added thereto, followed by extraction with diethyl ether. The organic layer was washed with a saturated sodium chloride solution, dried with anhydrous sodium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (elution solvent; hexane:ethyl acetate=4:1) to obtain methyl 4-ethoxy-3-fluorophenyldithiocarbamate (2.5 g, 10 mmol) as crystals. m.p. 108.0° C.

1. stirringThe mixture was stirred at room temperature for 10 hours
2. stirringThe mixture was stirred at room temperature for 30 minutes
3. extractionfollowed by extraction with diethyl ether
4. washThe organic layer was washed with a saturated sodium chloride solution
5. dry with materialdried with anhydrous sodium sulfate
6. concentrationconcentrated under reduced pressure
7. washThe residue was subjected to silica gel column chromatography (elution solvent; hexane:ethyl acetate=4:1)

ORDレコード

ord-2f23f47c1e144a8495d530761ecefd76

出典データセット

uspto-grants-1999_01

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05863932