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HRID 1802作成日:2026年10月24日

Acetic Acid → Pivalaldehyde

https://huagongshe.com/ja/reaction/1802

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物2-Amino-5-bromo-alpha-(2-pyridyl)benzyl alcoholHCID 12915500—
生成物PivalaldehydeHCID 12417—
生成物2-Amino-5-bromo-alpha-(2-pyridyl)benzyl alcoholHCID 12915500—

反応手順

In 20 ml of acetic acid was dissolved 2.0 g of 2-amino-5-bromo-α-(2-pyridyl)benzyl alcohol obtained in (1) together with 0.86 ml of trimethylacetoaldehyde. To the solution was added 0.36 g of sodium borohydride under ice-cooling. The reaction mixture was stirred for 30 minutes at room temperature and then subjected to extraction with a mixture of 100 ml of water and 150 ml of ethyl acetate. The ethyl acetate layer was washed with 1N sodium hydroxide, dried over anhydrous magnesium sulfate, and concentrated to dryness under reduced pressure. The residue was purified by silica gel column chromatography (eluent, hexane:ethyl acetate=5:1) to afford 5-bromo-2-neopentylamino-α-(2-pyridyl)benzyl alcohol (2.4 g) as an oily product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726306
出典データセットuspto-grants-1998_03
ORD IDord-5873d336793841adad5cbcf873b625c5
出典メモuspto-grants-1998_03