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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13886생성일: 2026년 10월 26일

Chlorobenzene → Triphenylamine

https://huagongshe.com/reaction/13886

반응식

참여 물질

역할이름HCID투입량
반응물ChlorobenzeneHCID 7964—
반응물DiphenylamineHCID 11487—
반응물Sodium t-butoxideHCID 23676156—
촉매palladium(II) acetateHCID 167845—
촉매Tri-tert-butylphosphonium TetraphenylborateHCID 23136663—
용매O-XyleneHCID 7237—
생성물TriphenylamineHCID 1177591.8%

반응 단계

A 100-ml four-necked flask was equipped with a stirrer, a thermometer and a reflux condenser. 5.403 g (48 mmol) of chlorobenzene, 6.769 g (40 mmol) of diphenylamine, 4.613 g (48 mmol) of sodium-tert-butoxide, 0.002 g (0.01 mmol) of palladium (II) acetate and 5 ml of xylene were weighed in the flask, followed by stirring. Further, 0.021 g (0.04 mmol) of tri-tert-butylphosphonium tetraphenylborate obtained in Example A-1 was weighed in air and added into the flask. The flask was purged with argon, followed by stirring at 100-120° C. for 10 hours. After the completion of the reaction, 45 ml of xylene and 50 ml of saturated sodium chloride solution were added, followed by separation. The organic phase was purified by column chromatography to afford 9.008 g of triphenylamine (yield: 92 mol % based on diphenylamine). The melting point was 125-126° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728176B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-6c6131f7f7fc4152b71a387511cff45e
출처 메모uspto-grants-2010_06