HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1449577Erstellt: 25. Oktober 2026
Carbon Dioxide → 2-(tert-Butoxycarbonyl)-6-chloro-4-trifluoromethylbenzoic acid
https://huagongshe.com/reaction/1449577
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | tert-butyl N-[3-chloro-5-(trifluoromethyl)phenyl]carbamate | HCID 18929880 | — |
| Edukt | HCID 178418306 | HCID 178418306 | — |
| Lösungsmittel | Pentane | HCID 8003 | — |
| Produkt | 2-(tert-Butoxycarbonyl)-6-chloro-4-trifluoromethylbenzoic acid | HCID 18929947 | 82% |
Reaktionsschritte
To a cold (-100° C.) stirred solution of N-(tert-butoxycarbonyl)-3-chloro-5-trifluoromethylaniline 93.4 g, 11.5 mM) in dry tetrahydrofuran (30 mL) under a nitrogen atmosphere was added dropwise t-butyllithium (14.2 mL of 1.7M solution, 24.2 mM) in pentane. The temperature of the reaction mixture was maintained at -103° to -98° C. during the addition and for 3.25 hr after the addition was completed. Crushed Dry Ice was then added to the cold reaction mixture which, after being allowed to warm to -75° C., was poured into water. The resulting mixture was extracted with ethyl acetate and the combined extracts were dried (MgSO4), filtered and concentrated to leave (3.2 g, 82%) the title compound as a solid white foam.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05599814 |
|---|
| Quelldatensatz | uspto-grants-1997_02 |
|---|
| ORD ID | ord-fbe886a1c4e449dc8d59f3693e9f7c69 |
|---|
| Quellennotiz | uspto-grants-1997_02 |
|---|