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HRID 10118作成日:2026年10月26日

4-Hydroxybenzoic Acid → 4-(6-Hydroxyhexyloxy)benzoic acid

https://huagongshe.com/reaction/10118

反応式

関与物質

役割名称HCID仕込み量
反応物4-Hydroxybenzoic AcidHCID 135—
反応物6-Chloro-1-hexanolHCID 74828—
溶媒Potassium HydroxideHCID 14797—
生成物4-(6-Hydroxyhexyloxy)benzoic acidHCID 362841380%

反応条件

温度60 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094358B2
出典データセットuspto-grants-2006_08
ORD IDord-dfe4ced729254e01be55cc9bea0175d5
出典メモuspto-grants-2006_08