HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-(Methoxymethylidene)-3,4-dihydronaphthalen-1(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1-oxo-1,2,3,4-tetrahydronaphthalene-2-carbaldehyde | HCID 10374913 | — |
| Product | 2-(Methoxymethylidene)-3,4-dihydronaphthalen-1(2H)-one | HCID 53658781 | — |
Reaction Steps
The 2-formyl-1-tetralone derivative of formula (3) is converted to the corresponding 2-enol ether of formula (4) by reacting a compound of formula (3) with an alcohol, preferably methanol, in the presence of a catalytic amount of a strong acid, preferably concentrated sulfuric acid. The reaction is preferably carried out at a temperature of about the reflux temperature of the alcohol, for about 5 minutes to 2 hours, preferably about 15 minutes. The product of formula (4), a 2-methoxymethylene-1-tetralone derivative, is isolated by conventional means, preferably by precipitation and filtration, and is reacted in the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753663 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-3968a2ffc71446c992a316728d460ea7 |
| Source note | uspto-grants-1998_05 |