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HRID 971834作成日:2026年10月26日
6-tert-Butyl-3-(chloromethyl)-2,4-dimethylphenol → Di-n-octadecyl 4-tert.-butyl-2,6-dimethyl-3-hydroxybenzylphosphonate
https://huagongshe.com/reaction/971834
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 6-tert-Butyl-3-(chloromethyl)-2,4-dimethylphenol | HCID 90131 | — |
| 反応物 | Phosphorous acid, trioctadecyl ester | HCID 248442 | — |
| 生成物 | Di-n-octadecyl 4-tert.-butyl-2,6-dimethyl-3-hydroxybenzylphosphonate | HCID 21311760 | — |
反応手順
21.7 Grams of trioctadecyl phosphite and 5.75 grams 6-tert.-butyl-3-chloromethyl-2,4-dimethylphenol was stirred together as a melt at 110° to 120° for 2 hours and at 120° to 125° for 7 hours. The reaction mixture was dissolved in 100 ml. of toluene and the colorless, slightly turbid solution was successively washed with 3 N aqueous hydrochloric acid, water, 2 N aqueous sodium carbonate solution and water until the wash waters were neutral. After drying over anhydrous sodium sulfate and filtering free of drying agent, the clear filtrate was concentrated by distillation of the solvent at reduced pressures. The residual oil was topped in the "ASCO 50" Rota-Film Molecular Still at a wall temperature of 210° to 215° and a pressure of 1 to 5 microns. After crystallization from methylethyl ketone, the desired product was obtained as white crystals melting at 70° to 72.5°. (compound 4)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04161473 |
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| 出典データセット | uspto-grants-1979_07 |
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| ORD ID | ord-e8710ffcc8bc4168a51c36b83530d5fb |
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| 出典メモ | uspto-grants-1979_07 |
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