참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Carbon Disulfide | HCID 6348 | — |
| 반응물 | Zinc Acetate | HCID 11192 | — |
| 반응물 | 2,2-Dimethyl-oxazolidine | HCID 550697 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | Zinc Bis(2,2-dimethyloxazolidine-3-carbodithioate) | HCID 21453996 | — |
반응 단계
While cooling and stirring, 20 g. (0.20 mole) of 2,2-dimethyloxazolidine (preparation described by E. Bergmann et. al., J. Am. Chem. Soc. 75, 358 (1953)) was added to a solution of 15.2 g. (0.20 mole) carbon disulfide in 150 g. pyridine. To the stirring solution was added 18.3 g. (0.10 mole) of anhydrous zinc acetate at 25°-30°C. After standing overnight at room temperature, filtration gave 15.2 g. of the crude product; vacuum-concentration of the filtrate and ethanol-dilution of the residue gave an additional 10.4 g. After combining and vacuum-drying of the crude product at 100°C there was obtained 17.8 g. of the desired carbodithioate melting at 188°- 190°C (decomp.). A small sample, dissolved in hot chloroform and precipitated by hexane (m. 192°- 3°C decomp.) had the following analysis: Found: C, 34.22; H, 4.47; N, 6.84; Zn, 15.20%. Calcd for C12H20N2O2S 4 Zn: C, 34.50; H, 4.79; N, 6.71; Zn, 15.67%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US03943143 |
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| 출처 데이터셋 | uspto-grants-1976_03 |
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| ORD ID | ord-926e339cb26d43fe879fbd7d6cc04b66 |
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| 출처 메모 | uspto-grants-1976_03 |
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