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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1272148생성일: 2026년 10월 26일

Diethyl disulfide → (4R,9aR)-7-Ethylsulfanyl-4,6-dimethyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1272148

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl disulfideHCID 8077—
반응물(4R,9aR)-7-Bromo-4,6-dimethyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl esterHCID 69357585—
반응물HCID 178418306HCID 178418306—
용매Diethyl EtherHCID 3283—
생성물(4R,9aR)-7-Ethylsulfanyl-4,6-dimethyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl esterHCID 6935656157.2%

반응 조건

온도-78 °C

반응 단계

A solution of 0.50 g (1.31 mmol) (4R,9aR)-7-bromo-4,6-dimethyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester (example 6, intermediate) in 30 mL diethyl ether was cooled to −100° C. and 1.05 mL tert-butyl-lithium (1.57 mmol; 1.5M solution in n-pentane) was added dropwise. After 15 min. diethyl disulfide was added and the reaction was stirred at −78° C. for 1 h. The reaction mixture was quenched with 10% aqueous citric acid solution and extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and evaporated. The residue was purified by column chromatography over silica gel (0.030–0.063 mm) with ethyl acetate:n-hexane (1:4) as eluant to give the product as a light yellow solid (57.2%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07208494B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-5320ad194d7f49fe92bb407770f5d305
출처 메모uspto-grants-2007_04