関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Butoxyphenol | HCID 31233 | — |
| 反応物 | 4-{[6-(Methacryloyloxy)hexyl]oxy}benzenecarboxylic acid | HCID 3730344 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | 4-(6-Methacryloyloxyhexyloxy)-benzoic acid-4-n-butoxyphenyl ester | HCID 19431246 | — |
反応手順
6.1 g of 4-(6-methacryloyloxyhexyloxy)benzoic acid were converted to the acid chloride in a manner similar to example 6. This substance was taken up in 100 ml of tetrahydrofuran (THF) and added dropwise at 0° to 5° C. to a stirred solution of 3.3 g of hydroquinone monobutyl ether in 100 ml of THF and 4 ml of triethylamine. The mixture was stirred for a further 3 hours at room temperature and the triethylamine hydrochloride was then filtered out. The filtrate was evaporated to dryness and the residue dissolved in 50 ml of dichloromethane. The solution was washed several times with water, dried with sodium sulphate and the solvent then distilled off. The crude product so obtained was purified by column chromatography and recrystallisation from n-hexane.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05543267 |
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| 出典データセット | uspto-grants-1996_08 |
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| ORD ID | ord-976b6cb7b19143f094aa497e49fe319a |
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| 出典メモ | uspto-grants-1996_08 |
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