関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Dimethyl Succinate | HCID 7820 | — |
| 反応物 | Lithium amide | HCID 24532 | — |
| 反応物 | 4-Hydroxy-2,2,6,6-tetramethylpiperidine | HCID 75471 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | Bis(2,2,6,6-tetramethyl-4-piperidyl) succinate | HCID 93340 | — |
反応手順
322.3 g (2.05 mol) of 4-hydroxy-2,2,6,6-tetramethylpiperidine and 146.1 g (1 mol) of dimethyl succinate in 300 ml of xylene are heated to 80° C. 1.2 g of lithium amide are added to the reaction mixture at this temperature, and the temperature is raised to 120°-125° C. A mixture of methanol and xylene is then distilled off slowly under a slow stream of nitrogen. After approx. 10 hours virtually no more methanol distills off, which indicates the end of the transesterification. The contents of the flask are diluted with 500 ml of petroleum ether (boiling range 110°-140° C.) and are washed in the separating funnel while still warm (60°-70° C.) with three times 100 ml of water. The reaction product crystallizes from the organic phase on cooling as colourless crystals. The di-(2,2,6,6-tetramethyl-4-piperidinyl) succinate obtained melts at 118° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05028645 |
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| 出典データセット | uspto-grants-1991_07 |
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| ORD ID | ord-e2c57bcea7324b6b970ab5deb54a3144 |
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| 出典メモ | uspto-grants-1991_07 |
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