HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide dimethyl acetal → HCID 178468532, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | Ethyl 3-amino-7-(2-chloroethoxy)-6-methoxy-2-naphthoate | HCID 9858408 | — |
| Reactant | Ethyl 3-amino-6-(2-chloroethoxy)-7-methoxy-2-naphthoate | HCID 11594979 | — |
| Product | HCID 178468532 | HCID 178468532 | — |
| Product | HCID 178468534 | HCID 178468534 | — |
Reaction Steps
A 648 mg portion of ethyl 3-amino-7-(2-chloroethoxy)-6-methoxy-2-naphthoate and ethyl 3-amino-6-(2-chloroethoxy)-7-methoxy-2-naphthoate (1:1 mixture) and 5 mL of dimethylformamide dimethylacetal is heated to reflux using an oil bath. The reaction is kept at reflux overnight. Solvent is removed in vacuo to provide crude ethyl 6-(2-chloroethoxy)-3-{[(E)-(dimethylamino)methylidene]amino}-7-methoxy-2-naphthoate and ethyl 7-(2-chloroethoxy)-3-{[(E)-(dimethylamino)-methylidene]amino}-6-methoxy-2-naphthoate (1:1 mixture) as a dark red mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105531B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-98c71b6d1e324af88dd3b6f49fb63ff7 |
| Source note | uspto-grants-2006_09 |