Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Sodium Iodide → Dimesityl disulfide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | 2-Mesitylenesulfonyl chloride | HCID 13046 | — |
| 반응물 | Acetic acid, 2-fluoro-, 1,1'-anhydride | HCID 67886 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | Dimesityl disulfide | HCID 345613 | — |
반응 단계
2,4,6-trimethylphenylsulfonyl chloride (500 mg, 2.3 mmol) was dissolved in acetone (60 mL), and then NaI (3.4 g, 23 mmol) and fluoroacetic anhydride (1.45 mL, 6.9 mmol) were added and the mixture was stirred at room temperature for one hour. The reaction solution was concentrated, water was added, extraction was performed with ether and the organic layer was further washed with aqueous sodium thiosulfate, water and saturated saline. After drying over magnesium sulfate and vacuum concentration, the residue was purified with a silica gel column (hexane) to obtain 2,4,6-trimethylphenyldisulfide as a light yellow crystalline compound (231 mg, 0.76 mmol, 67% yield). The NMR and mass spectral data for the obtained compound were as follows:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06900307B1 |
| 출처 데이터셋 | uspto-grants-2005_05 |
| ORD ID | ord-66600d1abbe64ed2958ff894b380c2be |
| 출처 메모 | uspto-grants-2005_05 |