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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2859생성일: 2026년 10월 24일

Hydroxyamine hydrochloride → (+/-)-trans-2-Ethyl-6-hydroxyimino-4a-(3-methoxyphenyl)-1,2,3,4,4a,5,6,7,8, 8a-decahydroisoquinoline

https://huagongshe.com/ko/reaction/2859

반응식

참여 물질

역할이름HCID투입량
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물(+/-)-trans-2-Ethyl-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8,8a-decahydroisoquinoline hydrochlorideHCID 86752325—
용매MethanolHCID 887—
생성물(+/-)-trans-2-Ethyl-6-hydroxyimino-4a-(3-methoxyphenyl)-1,2,3,4,4a,5,6,7,8, 8a-decahydroisoquinolineHCID 8675232496.6%

반응 단계

0.5 g (1.54 mmol) of (±)-trans-2-ethyl-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8,8a-decahydroisoquinoline hydrochloride, 0.456 g (6.56 mmol) of hydroxylamine hydrochloride and 0.64 g of KHCO3 in 10 ml of MeOH were refluxed for 45 min. The precipitate was filtered, the solvent was removed in vacuo and the residue taken up in H2O. The pH was adjusted to 8 with conc. NH4OH, the aqueous layer was extracted with CH2Cl2. The organic layer was dried, the solvent removed in vacuo, obtaining 0.45 g of the title compound which was used as such in the subsequent step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731322
출처 데이터셋uspto-grants-1998_03
ORD IDord-4eac917dd565431a9f46b59b364b582d
출처 메모uspto-grants-1998_03