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HRID 541207作成日:2026年10月27日

p-Toluenesulfonic acid → Methyl oxolane-3-carboxylate

https://huagongshe.com/reaction/541207

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物(R)-Tetrahydro-3-furoic acidHCID 4661317—
溶媒MethanolHCID 887—
生成物Methyl oxolane-3-carboxylateHCID 106782635,122.6%

反応手順

A solution of tetrahydrofuran-3-carboxylic acid (540 mg, 4.65 mmol, 1.00 equiv) and TsOH (10 mg, 0.06 mmol, 0.01 equiv) in methanol (40 mL) was stiffed at 66° C. in an oil bath. After 16 h, the resulting mixture was cooled to room temperature and concentrated under reduced pressure. The residue was dissolved in 10 mL of ether, washed with 1×20 mL of NaHCO3 (aq., sat.) followed by 3×20 mL of brine, and concentrated under reduced pressure to yield 0.40 g (66%) of the title compound as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871790B2
出典データセットuspto-grants-2014_10
ORD IDord-01dd4c6476c5410eb28962ad379a19c2
出典メモuspto-grants-2014_10