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HRID 1779872作成日:2026年10月26日

Benzyl Alcohol → 2-Furancarboxylic acid, tetrahydro-, phenylmethyl ester

https://huagongshe.com/reaction/1779872

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl AlcoholHCID 244—
反応物PyridineHCID 1049—
反応物Tetrahydro-2-furancarbonyl chlorideHCID 551254—
溶媒Diethyl EtherHCID 3283—
生成物2-Furancarboxylic acid, tetrahydro-, phenylmethyl esterHCID 11287208—

反応手順

Tetrahydrofuroyl chloride (15.0 g, 112 mmol) was added dropwise to a cold solution of benzyl alcohol (10.9 g, 101 mmol) and pyridine (20.0 g, 253 mmol) in Et2O (200 mL). The solution was stirred at 0° for 40 minutes, then filtered to remove the side product pyridine hydrochloride. The filtrate was washed with 0.1M HCl (50 mL), saturated aqueous NaHCO3 (50 mL), and brine (50 mL), and then dried over MgSO4. Filtration and evaporation of the solvent gave a yellow oil, which was distilled. Benzyl tetrahydrofuroate was obtained as a colorless oil (21.1 g), b.p. 118° to 120° at 0.5 mm Hg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05628980
出典データセットuspto-grants-1997_05
ORD IDord-1f9b60caca7c4d5cb481bbf00fbc0584
出典メモuspto-grants-1997_05