戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 839525作成日:2026年10月25日

Carbon Dioxide → 2-Methyl-3-Hydroxy-4-Hydroxymethyl-5-Fluoromethyl-Pyridine

https://huagongshe.com/reaction/839525

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物Hydrochloric AcidHCID 313—
反応物PyridoxineHCID 1054—
反応物Sulfur tetrafluorideHCID 24555—
反応物Acetone cardiceHCID 18522661—
反応物HCID 178477758HCID 178477758—
生成物2-Methyl-3-Hydroxy-4-Hydroxymethyl-5-Fluoromethyl-PyridineHCID 12510818—

反応手順

Sulfur tetrafluoride (41 mg.-mole) is passed into 40 ml. of liquid HF, cooled in a dry-ice-acetone bath, then, acetonide of 2-methyl-3-hydroxy-4-hydroxymethyl-5-hydroxymethyl pyridine, (4.18 g.; 20 mg.-mole) is added under continuing cooling. The dry-ice-acetone bath is not replenished with dry-ice and the mixture is left standing in it overnight. After blowing off the remaining HF at room temperature, conc. aq. HCl is added, evaporated to dryness in vacuo, the residue is redissolved in 20 ml. of 1M aq. HCl, heated on the steam-bath for 15 minutes, (for hydrolysis of the acetonide, charcoaled and evaporated to dryness, redissolved in water, then passed through a Dowex 50 × 2 cation-exchange resin column, washed free of F⃝ with water.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04096180
出典データセットuspto-grants-1978_06
ORD IDord-123d7525db764acab27efe24f1d2c49f
出典メモuspto-grants-1978_06