HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1453782Erstellt: 26. Oktober 2026
N,N-dimethyl-1-naphthylamine → 1-(Isocyanatomethyl)-4-(propan-2-yloxy)benzene
https://huagongshe.com/reaction/1453782
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | N,N-dimethyl-1-naphthylamine | HCID 6848 | — |
| Edukt | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Edukt | Benzeneacetic acid, 4-(1-methylethoxy)- | HCID 799528 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(Isocyanatomethyl)-4-(propan-2-yloxy)benzene | HCID 57430095 | 112,3% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07476682B2 |
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| Quelldatensatz | uspto-grants-2009_01 |
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| ORD ID | ord-6d5bb36fcd044070911f2bc5ccdb3479 |
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| Quellennotiz | uspto-grants-2009_01 |
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