HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethyl bromoacetate → 2-(Carboxymethoxy)thioxanthone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethyl bromoacetate | HCID 7748 | — |
| Edukt | 2-Hydroxy-9H-thioxanthen-9-one | HCID 9794568 | — |
| Produkt | 2-(Carboxymethoxy)thioxanthone | HCID 3019853 | 75% |
Reaktionsschritte
An example of a conventional synthetic route to 2-carboxymethoxythioxanthone involves three stages. Firstly, phenol is reacted with dithiobisbenzoic acid to produce 2-hydroxythioxanthone in a 60% yield. Secondly, the 2-hydroxythioxanthone is reacted with ethyl bromoacetate to produce the ethyl ester of 2-carboxymethoxythioxanthone in 75% yield. Thirdly, the ester is hydrolysed by acidification to produce the desired product in 90% yield. These three stages form an inefficient and time-consuming process to provide a product that is a dark colour, contains impurities and by-products and is produced with only an overall yield of 40% from the starting material.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06960668B2 |
| Quelldatensatz | uspto-grants-2005_11 |
| ORD ID | ord-e782f4331ec0437b9f66ccd6ca7fc05c |
| Quellennotiz | uspto-grants-2005_11 |