참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,2-Dibromoethane | HCID 7839 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Dimethylacetamide | HCID 31374 | — |
| 반응물 | Benzenemethanethiol, alpha,alpha-diphenyl- | HCID 77281 | — |
| 반응물 | 3-Buten-1-amine | HCID 443732 | — |
| 생성물 | Allyl-methyl-(2-tritylsulfanyl-ethyl)-amine | HCID 22568030 | — |
반응 단계
5.53 g (20 mmol) triphenylmethanethiol in 50 ml DMA were deprotonated at 0° C. with 0.87 g (20 mmol) of 55% NaH. The reaction was stirred for 30 min at RT, dropped slowly (30 min) to a cooled (0° C.) solution of 1.72 ml (20 mmol) of 1,2-dibromoethane in 50 ml DMA. The reaction mixture was stirred for 6 h at RT, cooled (0° C.) and treated with 3.83 ml (40 mmol) of N-allylmethylamine. After 16 h at RT, the reaction was cooled (0° C.) and treated again with 3.83 ml (40 mmol) of N-allylmethylamine. After 24 h at RT, the solution was concentrated and dissolved in aqueous saturated NaHCO3/Et2O (3×). The organic phase was dried over Na2SO4 and evaporated. Flash column chromatography on silica gel with CH2Cl2/MeOH (99.5:0.5 to 95:5) yielded 3.27 (44%) of Allyl-methyl-(2-tritylsulfanyl-ethyl)-amine, MS: 374 (MH+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07335687B2 |
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| 출처 데이터셋 | uspto-grants-2008_02 |
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| ORD ID | ord-929fd4f1f8ce4643bd7bb4c7a81459b5 |
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| 출처 메모 | uspto-grants-2008_02 |
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