참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diiodomethane | HCID 6346 | — |
| 반응물 | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| 반응물 | Sodium Sulfite | HCID 24437 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Diethylether hexane | HCID 21584099 | — |
| 생성물 | 1-Bromo-4-iodomethanesulfonyl-benzene | HCID 68515285 | — |
반응 단계
A stirred mixture of 4-bromo-benzenesulfonyl chloride (5.12 g, 20 mmol), sodium sulfite (4.69 g, 37.3 mmol) and sodium bicarbonate (3.07 g, 36.6 mmol) in water (20 mL) is heated at 100° C. for 1 h. The crude sodium sulfinate solution is allowed to cool for 30 min and then treated with diiodomethane (25 mL) and tetra-N-butyl ammonium bromide (0.65 g, 2.0 mmol). The resulting mixture is heated at 75° C. overnight. The organic layer was separated. The aqueous solution was extracted with CH2Cl2 (×2). The combined organics were washed with water and brine, and dried over anhydrous MgSO4. The filtration through Celite-silica gel pad and concentration in vacuo gave light yellow liquid residue. Et2O/hexane (1:1) was added to the residue and the mixture was stirred to make homogenous and sit at 0 C for 20 min. The product was crushed out of the solution, filtered and washed with Et2O/hexanes. 1H NMR (300 MHz, CDCl3) 7.83 (d, 2H), 7.75 (d, 2H), 4.48 (s, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07803793B2 |
|---|
| 출처 데이터셋 | uspto-grants-2010_09 |
|---|
| ORD ID | ord-d0f850389543494caa9e470c838c9435 |
|---|
| 출처 메모 | uspto-grants-2010_09 |
|---|