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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1390481생성일: 2026년 10월 25일

2,2-Dimethylvaleroyl chloride → HCID 86736301, 화합물

https://huagongshe.com/reaction/1390481

반응식

참여 물질

역할이름HCID투입량
반응물2,2-Dimethylvaleroyl chlorideHCID 519171—
반응물HCID 86736302HCID 86736302—
용매2,2-Dimethylpentanoic acidHCID 14455—
생성물HCID 86736301HCID 86736301—

반응 단계

Using a procedure similar to that described above in Example 3A, 3,4-dihydroxyphenyl N-benzyl-N-methylaminomethyl ketone methanesulfonate is reacted with two mole equivalents of 2,2-dimethylpentanoyl chloride in 2,2-dimethylpentanoic acid to yield 3,4-bis(2,2-dimethylpentanoyloxy)phenyl N-benzyl-N-methylaminomethyl ketone methanesulfonate as a white crystalline solid. This salt is debenzylated by catalytic hydrogenation in the presence of palladium-on-charcoal hydrogenation catalyst, in the same manner as the debenzylation procedure described above in Example 124, to yield 3,4-bis(2,2-dimethylpentanoyloxy)phenyl methylaminomethyl ketone methanesulfonate as a white crystalline solid. This salt is catalytically hydrogenated in anhydrous ethyl alcohol in the presence of 10 percent palladium-on-charcoal hydrogenation catalyst until one mole equivalent of hydrogen is absorbed. There is thus obtained 3,4-bis(2,2-dimethylpentanolyoxy)-alpha-(methylaminomethyl)benzyl alcohol methanesulfonate as a white crystalline solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04138581
출처 데이터셋uspto-grants-1979_02
ORD IDord-a87a910d9af84706807d27c81b829d67
출처 메모uspto-grants-1979_02