참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 1-Iodo-2-methoxyethane | HCID 79136 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | Tert-butyl 1,3-dithiane-2-carboxylate | HCID 86007917 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Tert-butyl 2-(2-methoxyethyl)-1,3-dithiane-2-carboxylate | HCID 90060334 | — |
반응 단계
10.2 g (46.1 mmol) of tert-butyl 1,3-dithiane-2-carboxylate and 12.0 g (64.5 mmol) of 1-iodo-2-methoxyethane were initially charged in 127 ml of dimethylformamide, the mixture was cooled to 0° C. and 6.21 g (55.3 mmol) of potassium tert-butoxide were added. The resulting reaction mixture was stirred at 0° C. for 1 h and at RT for 16 h. The reaction mixture was added to 1.5 l of a 1:2 mixture of ice and saturated aqueous ammonium chloride solution and extracted three times with 300 ml of diethyl ether. The combined organic phases were dried over magnesium sulphate and filtered, and the solvent was removed under reduced pressure. The crude product was used for the next step without further purification. Yield: 11.1 g (87% of theory)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09434690B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-23e59bb0f1e44d93a51a2c618ff37b6d |
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| 출처 메모 | uspto-grants-2016_09 |
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