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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1802생성일: 2026년 10월 23일

Acetic Acid → Pivalaldehyde

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

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물2-Amino-5-bromo-alpha-(2-pyridyl)benzyl alcoholHCID 12915500—
생성물PivalaldehydeHCID 12417—
생성물2-Amino-5-bromo-alpha-(2-pyridyl)benzyl alcoholHCID 12915500—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726306
출처 데이터셋uspto-grants-1998_03
ORD IDord-5873d336793841adad5cbcf873b625c5
출처 메모uspto-grants-1998_03