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Chemical Structure| 627-01-0 Chemical Structure| 627-01-0
Chemical Structure| 627-01-0

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Synonyms: N-Ethylglycine

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Product Details of N-Et-Gly-OH

CAS No. :627-01-0
Formula : C4H9NO2
M.W : 103.12
SMILES Code : CCNCC(O)=O
Synonyms :
N-Ethylglycine
MDL No. :MFCD00037794
InChI Key :YPIGGYHFMKJNKV-UHFFFAOYSA-N
Pubchem ID :316542

Safety of N-Et-Gly-OH

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of N-Et-Gly-OH

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 627-01-0 ]

[ 627-01-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 627-01-0 ]
  • [ 175205-39-7 ]
  • 1-ethyl-3-(5-fluoro-2-methylphenyl)-2-thioxo-imidazolidin-4-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In diethyl ether; ethanol; chloroform; ethyl acetate; EXAMPLE 28 1-Ethyl-3-(5-fluoro-2-methylphenyl)-2-thioxo-imidazolidin-4-one A mixture of the crude N-ethyl glycine (11.5 g), 5-fluoro-2-methylphenylisothiocyanate (10.42 g), triethylamine (12.5 g) and chloroform (300 mL) was heated at reflux for 6 hours. The solvent was evaporated. The residue was dissolved in ethyl acetate (500 mL) and washed with water (500 mL). The organic phase was evaporated to dryness. The residue was dissolved in ethanol (50 mL), then diluted with diethyl ether (200 mL). The solution was saturated with hydrogen chloride. The mixture was filtered. The solid was discarded. The filtrate was evaporated to dryness. The residue was dissolved in diethyl ether (300 mL) and washed with water (200 mL). The organic phase was dried over anhydrous sodium sulfate and evaporated to dryness. Crystallization from ethanol afforded the title compound (6.5 g) as a pink solid, m.p. 98-100 C. Anal. Calcd. for. C12 H13 F N2 O S: C, 57.13; H, 5.19; N, 11.10. Found: C, 56.88; H, 5.17; N, 11.05. Mass spectrum (EI, M.+) m/z 252.
With triethylamine; In diethyl ether; ethanol; chloroform; ethyl acetate; EXAMPLE 7 1-Ethyl-3-(5-fluoro-2-methylphenyl)-2-thioxo-imidazolidin-4-one A mixture of the crude N-ethyl glycine (11.5 g), 5-fluoro-2-methylphenyl-isothiocyanate (10.42 g), triethyl amine (12.5 g) and chloroform (300 mL) was heated at reflux for 6 hours. The solvent was evaporated. The residue was dissolved in ethyl acetate (500 mL) and washed with water (500 mL). The organic phase was evaporated to dryness. The residue was dissolved in ethanol (50 mL), then diluted with diethyl ether (200 mL). The solution was saturated with hydrogen chloride. The mixture was filtered. The solid was discarded. The filtrate was evaporated to dryness. The residue was dissolved in diethyl ether (300 mL) and washed with water (200 mL). The organic phase was dried over anhydrous sodium sulfate and evaporated to dryness. Crystallization from ethanol afforded the title compound (6.5 g) as a pink solid, m.p. 98-100 C. Anal. Calcd. for. C12 H13 F N2 O S: C, 57.13; H, 5.19; N, 11.10. Found: C, 56.88; H, 5.17; N, 11.05. Mass spectrum (EI, M.+) m/z 252.
 

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