참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Bromoacetic Acid | HCID 6227 | — |
| 반응물 | Carbon Disulfide | HCID 6348 | — |
| 반응물 | 2,4-Dimethylaniline | HCID 7250 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 3-(2,4-Dimethyl-phenyl)-2-thioxo-thiazolidin-4-one | HCID 1907856 | — |
반응 단계
At 0° C., 1 g of 2,4-dimethylaniline (8.04 mmol) was mixed with 54 mL of a 0.2 M solution of triethylamine in ethyl acetate, and 0.65 mL of a carbon disulfide (CS2) solution was dropwise added to the mixture with slowly stirring. After completion of the addition, stirring was continued for an additional 12 hrs. The reaction mixture was filtered, and the filtrate was dissolved in an aqueous sodium bicarbonate solution (NaHCO3) and mixed with 2.2. g of bromoacetic acid (15.83 mmol) for 2 hrs by stirring. The resulting reaction mixture was acidified (pH 2) with a 35% HCl solution and heated for 6 hrs. After extraction with methylene chloride (CH2Cl2), the organic layer was pooled, washed with saturated brine, dried over magnesium sulfate, and concentrated in vacuo. Purification of the concentrate by silica gel column chromatography afforded the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08759536B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-0b10980121a141bf922a51ef83b85ead |
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| 출처 메모 | uspto-grants-2014_06 |
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