돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1657543생성일: 2026년 10월 27일

p-Menthan-3-one → Piperitenone

https://huagongshe.com/reaction/1657543

반응식

참여 물질

역할이름HCID투입량
반응물p-Menthan-3-oneHCID 6986—
반응물MenthoneHCID 26447—
생성물PiperitenoneHCID 38115264.6%

반응 단계

A similar process is described by S. Ohshiro et al (Yakugaku Zasshi, 88, 417 (1968)). Here again the reaction of methyl vinyl ketone with excess mesityl oxide takes place in the presence of potassium hydroxide powder but without addition of tetrahydrofuran as the solvent. The piperitenone obtained is converted into a mixture of menthone and isomenthone by catalytic hydrogenation. However, in this process of yields of piperitenone are again only about 53%; furthermore, using this process the menthone/isomenthone mixture is obtained in only 64.6% yield and in a purity of only 89.8%. For this reason, the further reaction to give pure methol has to be carried out in an involved manner via menthone-oxime (Jap. Pat. No. 7,009,375) and menthylamine, which makes it doubtful whether the process is suitable for commercial operation.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03960970
출처 데이터셋uspto-grants-1976_06
ORD IDord-5299a2cba2b041ffb03ebb7219d2590a
출처 메모uspto-grants-1976_06