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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 425266생성일: 2026년 10월 27일

Acetic Acid → Borane;2-methylpyridine

https://huagongshe.com/reaction/425266

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참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물BoraneHCID 6331—
반응물3-MethylpyridineHCID 7970—
반응물4-EthylpyridineHCID 10822—
반응물3-EthylpyridineHCID 10823—
반응물2-PropylpyridineHCID 69320—
반응물Borane;pyridineHCID 2723995—
용매PyridineHCID 1049—
생성물Borane;2-methylpyridineHCID 16217944—
생성물HCID 178419164HCID 178419164—
생성물HCID 178419168HCID 178419168—
생성물HCID 178419174HCID 178419174—

반응 단계

Pyridine forms an amine borane that is not moisture sensitive and very useful for reductive aminations and reductions in protic media. Pyridine borane is commercially available and often used in acetic acid to increase the reactivity of the borane. Unfortunately, it is thermally unstable and must be kept at temperatures less than 54° C. to avoid decomposition via hydroboration/polymerization processes. Its shelf-life at ambient temperature is only 6 months, Borane complexes of pyridine, 2-n-propylpyridine, 3-methylpyridine, 3-ethylpyridine and 4-ethylpyridine are liquids which violently decompose upon distillation (Mooney E. F. et al., J. Inorg. Nucl. Chem 1968, 30, p. 1439). 2-Picoline borane (mp. 50° C.), 2-ethylpyridine borane (mp, 50-51° C.), 2,6-lutidine borane (mp. 106-107° C.) and 2,4,6-collidine borane (mp. 99-100° C.) have been isolated as solids.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08106200B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-4d143ad01d254d1b85140b1240a70419
출처 메모uspto-grants-2012_01