HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl vanillate → Ethyl 3-methoxy-4-(naphth-2-ylmethoxy)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl vanillate | HCID 12038 | — |
| Reactant | 2-Bromomethylnaphthalene | HCID 70320 | — |
| Product | Ethyl 3-methoxy-4-(naphth-2-ylmethoxy)benzoate | HCID 19773143 | 54% |
Reaction Steps
2-Bromomethylnaphthalene was reacted with ethyl vanillate using the conditions described in Example 1 to give ethyl 3-methoxy-4-(naphth-2-ylmethoxy)benzoate in 54% yield, m.p. 86°-87° C. Following the procedures described in the portion of Example 6 which is concerned with the preparation of starting materials the product so obtained was reacted with thiazol-2-yl-lithium and the resultant product was reacted with ethylmagnesium iodide to give the required starting material as an oil in 20% yield, m.p. 124°-126° C. (recrystallised from a mixture of hexane and ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05196422 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-aa60acccb7b443cd9e3e26942e9787d7 |
| Source note | uspto-grants-1993_03 |