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HRID 1453782作成日:2026年10月27日

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

https://huagongshe.com/reaction/1453782

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-dimethyl-1-naphthylamineHCID 6848—
反応物P,P-Diphenylphosphinic azideHCID 199401—
反応物Benzeneacetic acid, 4-(1-methylethoxy)-HCID 799528—
溶媒TetrahydrofuranHCID 8028—
生成物1-(Isocyanatomethyl)-4-(propan-2-yloxy)benzeneHCID 57430095112.3%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07476682B2
出典データセットuspto-grants-2009_01
ORD IDord-6d5bb36fcd044070911f2bc5ccdb3479
出典メモuspto-grants-2009_01