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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1453782생성일: 2026년 10월 25일

N,N-dimethyl-1-naphthylamine → 1-(Isocyanatomethyl)-4-(propan-2-yloxy)benzene

https://huagongshe.com/reaction/1453782

반응식

참여 물질

역할이름HCID투입량
반응물N,N-dimethyl-1-naphthylamineHCID 6848—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물Benzeneacetic acid, 4-(1-methylethoxy)-HCID 799528—
용매TetrahydrofuranHCID 8028—
생성물1-(Isocyanatomethyl)-4-(propan-2-yloxy)benzeneHCID 57430095112.3%

반응 단계

1,8-Bis(dimethylaminonaphtalene (3.19 g, 14.9 mmol) was added to a solution of 4-(isopropoxy)phenyl acetic acid (2.89 g, 14.9 mmol) in dry tetrahydrofuran (18 mL) at rt under argon atmosphere. After 25 minutes stirring at rt diphenylphosphoryl azide (4.10 g, 14.9 mmol) was added dropwise and the mixture refluxed for 6 hours. It was allowed to cool to rt and then stored at −20° C. overnight to precipitate out the ammonium phosphate salt. A mixture of diethyl ether and ethyl acetate (1:1 v/v, 25 mL) was added to the cold reaction mixture. The precipitate was filtered from the reaction mixture and washed with diethyl ether: ethyl acetate (1:1 v/v, 20 mL). The filtrate was evaporated to dryness giving 1-isocyanatomethyl-4-isopropoxybenzene as an oil (3.2 g), which was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07476682B2
출처 데이터셋uspto-grants-2009_01
ORD IDord-6d5bb36fcd044070911f2bc5ccdb3479
출처 메모uspto-grants-2009_01