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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 622853생성일: 2026년 10월 26일

N-Acetylserotonin → Melatonin

https://huagongshe.com/reaction/622853

반응식

참여 물질

역할이름HCID투입량
반응물N-AcetylserotoninHCID 903—
반응물Dimethyl SulfateHCID 6497—
반응물Sodium HydroxideHCID 14798—
생성물MelatoninHCID 896—

반응 단계

To the aqueous alcoholic solution containing N-acetyl serotonine prepared in Example 2, there were added slowly and simultaneously 36 g of dimethyl sulphate and 20 g of 30% sodium hydroxide so that the pH was maintained at 12.5, while ensuring that the temperature did not exceed 40° C. During this operation, a part of the melatonine formed crystallised and this was filtered after neutralisation. The mother-liquor of crystallisation was decolourised with activated carbon, concentrated to eliminate the ethanol, then extracted with dichloromethane. After separation of the aqueous phase, the organic phase was concentrated to dryness which allowed the recuperation of a further 28 g of crude melatonine. The two fractions, which totalled 42 g, were mixed and purified by recrystallisation in a mixture containing water and ethanol in a 75:25 ratio. 30 g of white crystals of melatonine were obtained having a purity of 98.6%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04772726
출처 데이터셋uspto-grants-1988_09
ORD IDord-4f066a1441844658a9a20d9eb05f5e1a
출처 메모uspto-grants-1988_09