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HRID 26676作成日:2026年10月26日

Hydrochloric Acid → 2-[4-Hydroxy-3-(3-oxapentanoyl)phenyl]propan-1-ol

https://huagongshe.com/reaction/26676

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Ethyl PropionateHCID 7749—
反応物Sodium hydrideHCID 24758—
反応物2-(3-Acetyl-4-hydroxyphenyl)propan-1-olHCID 21322015—
溶媒HexamethylphosphoramideHCID 12679—
生成物2-[4-Hydroxy-3-(3-oxapentanoyl)phenyl]propan-1-olHCID 21322012—

反応手順

2-(3-Acetyl-4-hydroxyphenyl)propan-1-ol (15.0 g; 0.077 mol) was dissolved in hexamethylphosphoramide (150 ml) and slowly added to a stirred slurry of sodium hydride (10.0 g; 0.417 mol) in hexamethylphosphoramide (40 ml) at a rate sufficient to maintain the temperature below 25° C. Ethyl propionate (20.0 g; 0.2 mol) was added and the mixture stirred for 2 hours before pouring into 2N hydrochloric acid (600 ml). The solution was extracted with ether (2×300 ml) and the extracts evaporated to give 2-[4-hydroxy-3-(3-oxapentanoyl)phenyl]propan-1-ol as a yellow oil. This was dissolved in ethanol (100 ml) containing concentrated hydrochloric acid (20 ml) and the solution was refluxed for 30 mins. The ethanol was removed in vacuo and the aqueous phase extracted with chloroform (2×150 ml). The combined extracts were washed with saturated sodium bicarbonate solution and dried over magnesium sulphate. The solvent was removed and the resulting oil was chromatographed on a silica gel column using ether as eluent. Recrystallisation of the product using hexane/ether (2:1) furnished a white microcrystalline solid (5.0 g) mp 59.5°-60.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04151179
出典データセットuspto-grants-1979_04
ORD IDord-f67975b7b8cf4c7095418fff5fb2549b
出典メモuspto-grants-1979_04