関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Hydroxybenzoic Acid | HCID 135 | — |
| 反応物 | 6-Chloro-1-hexanol | HCID 74828 | — |
| 溶媒 | Potassium Hydroxide | HCID 14797 | — |
| 生成物 | 4-(6-Hydroxyhexyloxy)benzoic acid | HCID 3628413 | 80% |
反応手順
Monomers in which the bulky organic group was a t-butyl group and the alkyl groups were hexyl groups were made as follows. 4-hydroxybenzoic acid was dissolved in 30% ethanolic KOH. About 1% of KI was added as a catalyst. The mixture was heated to about 60° C. and a stoichiometric amount of 6-chloro-1-hexanol was slowly added over about ½ hour. After refluxing the reaction mixture for extended period of time (2-15 hrs) the contents was cooled, the reaction mixture was filtered off, and the filtrate solvent was evaporated under vacuum. Water was added into the residue and acidified with HCl and the precipitate was filtered and crystallized with ethanol, yielding approximately an 80% 4-(6-hydroxyhexyloxy)-benzoic acid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07094358B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-dfe4ced729254e01be55cc9bea0175d5 |
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| 出典メモ | uspto-grants-2006_08 |
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