関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methylamine | HCID 6329 | — |
| 反応物 | Tos-PEG4-t-butyl ester | HCID 60146205 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Methylamino-PEG3-t-butyl ester | HCID 53662991 | 87% |
反応手順
Into a 250-mL sealed bottle was placed a solution of tert-butyl 3-(2-(2-(2-(tosyloxy)ethoxy)ethoxy)ethoxy)propanoate (14 g, 32.41 mmol, 1.00 equiv) in tetrahydrofuran (5 mL) followed by CH3NH2 (66.9 g, 712.16 mmol, 21.98 equiv, 33% in ethanol) and the resulting solution was stirred overnight at 50° C. The resulting mixture was concentrated under vacuum, dissolved in 150 mL of dichloromethane and then washed with 2×150 mL of water and 1×150 mL of brine. The organic layer was dried over sodium sulfate and concentrated under vacuum to afford 8.2 g (87%) of tert-butyl 3-(2-(2-(2-(methylamino)ethoxy)ethoxy)ethoxy)propanoate as yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09289429B2 |
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| 出典データセット | uspto-grants-2016_03 |
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| ORD ID | ord-fbe1e532b2b946e6b3c0adfa813ef738 |
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| 出典メモ | uspto-grants-2016_03 |
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