참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-Ethyl-p-toluenesulfonamide | HCID 6637 | — |
| 반응물 | 1,3-Dichloropropane | HCID 8881 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-Ethyl-N-(3-chloropropyl)-p-toluenesulfonamide | HCID 14056762 | 42% |
반응 단계
To N-ethyl-p-toluenesulfonamide (5.01 g, 0.0251 mol) in DMF (50 mL) in a dry flask is added sodium hydride (80% in oil, 0.93 g, 0.031 mol). After gas evolution subsides, 1,3-dichloropropane (22.48 g, 0.199 mol) is added. The mixture is heated at 53° C. for 10 h then cooled and poured into ice water (300 mL), which is extracted twice with ether. The combined extracts are washed with 1% sodium bisulfite, water (3×), and brine. Removal of solvent by rotary evaporation then Kugelrohr distillation gives crude product, which is chromatographed on silica gel (30% hexane/CHCl3) to furnish 2.91 g product (42%) NMR (CDCl3) δ1.15 (t, 3H), 1.9-2.2 (m, 2H), 2.44 (s, 3H), 3.11-3.35 (m, 4H), 3.6 (t, 2H), 7.3 (d, 2H), 7.74 (d, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05681837 |
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| 출처 데이터셋 | uspto-grants-1997_10 |
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| ORD ID | ord-23c25065507e40958c562610e7847640 |
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| 출처 메모 | uspto-grants-1997_10 |
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