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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 917802생성일: 2026년 10월 26일

Terpinolene → N,N,N',N'-Tetra(3-methylphenyl)-9,10-diaminophenanthrene

https://huagongshe.com/reaction/917802

반응식

참여 물질

역할이름HCID투입량
반응물TerpinoleneHCID 11463—
반응물3-IodotolueneHCID 12268—
반응물Potassium HydroxideHCID 14797—
반응물N~9~,N~10~-Bis(3-methylphenyl)phenanthrene-9,10-diamineHCID 19347451—
촉매copper(I) bromideHCID 24593—
촉매Phosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
용매MeOH tetrahydrofuranHCID 21899815—
생성물N,N,N',N'-Tetra(3-methylphenyl)-9,10-diaminophenanthreneHCID 20734448—

반응 단계

9,10-Bis(3-methylanilino)phenanthrene was mixed in an amount of 6.6 g (17.0 mmol) with 14.8 g (68.0 mmol) of m-iodotoluene, 3.82 g (68 mmol) of potassium hydroxide, 0.98 g (6.8 mmol) of copper-(I) bromide, 2.52 g (6.8 mmol) of ethyltriphenylphosphonium bromide, and 10 mL of terpinolene. This mixture was reacted at 115-125° C. for 2 hours in a nitrogen stream. After the reaction, the reaction solvent was distilled off by vacuum concentration. To the residue were added 5 mL of toluene, 67 mL of ethyl acetate, and 22 mL of water. The resultant mixture was subjected to liquid separation. To the organic layer was added 71 mL of methanol. The resultant solution was cooled for crystallization. Thus, the target compound (I-22) was obtained as light-yellow crude crystals in an amount of 9.0 g (yield, 93.0%). The target compound obtained had a melting point of 223-224° C. and a content as determined by HPLC of 99.6% (HPLC conditions: column, YMC-A-312; eluent, methanol/tetrahydrofuran (V/V=99/1); detection UV, 254 nm; flow rate, 1.0 mL/min).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07273953B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-3f91ae5a596443c381e3e84785efddf8
출처 메모uspto-grants-2007_09