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HRID 53251作成日:2026年10月26日

Hydrochloric Acid → 3-Methoxypentane-1,5-diol

https://huagongshe.com/reaction/53251

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Methyl triflateHCID 9526—
反応物2,6-Di-tert-butylpyridineHCID 68510—
反応物Diethyl 3-hydroxyglutarateHCID 96259—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物3-Methoxypentane-1,5-diolHCID 22101218—

反応条件

温度-5 °C

反応手順

25 ml of methyl trifluoromethylsulfonate are added to a solution of 30 g of diethyl 3-hydroxyglutarate and 33 ml of 2,6-di-tert-butylpyridine in 500 ml of DCM and the mixture is refluxed for 5 hours. After cooling, 500 ml of a 0.5N solution of HCl are added, the organic phase is decanted and dried over magnesium sulfate and the solvent is evaporated off under vacuum. The solid obtained is taken up with 200 ml of anhydrous THF, the mixture is filtered and the filtrate is then cooled to -5° C. 160 ml of a 1M solution of lithium aluminum hydride in THF are then added slowly and the mixture is stirred for 16 hours, the temperature being allowed to rise to RT. The reaction mixture is cooled to 0° C. and 5.5 ml of water, 18 ml of a 15% solution of NaOH and 5.5 ml of water are added successively. The mineral salts are filtered off and the filtrate is evaporated under vacuum to give the expected product after distillation under reduced pressure. B.p.=104° C. under 1.5 Pa.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05618833
出典データセットuspto-grants-1997_04
ORD IDord-8afc1e24579042a999836fe21e456d14
出典メモuspto-grants-1997_04