HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 19773037, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Benzoic acid, 3,5-dihydroxy-, ethyl ester | HCID 20098 | — |
| Reactant | 2-Bromomethylnaphthalene | HCID 70320 | — |
| Product | HCID 19773037 | HCID 19773037 | 15% |
Reaction Steps
Ethyl 3,5-dihydroxybenzoate was reacted in turn with 2-bromomethylnaphthalene and allyl bromide using the conditions described in Example 1 to give ethyl 5-allyloxy-3-(naphth-2-ylmethoxy)benzoate in 15% yield, as an oil. Following the procedures described in the portion of Example 3 which is concerned with the preparation of starting materials the product so obtained was reacted with thiazol-2-yl-lithium to give 5-allyloxy-3-(naphth-2-ylmethoxy)phenyl 2-thiazolyl ketone in 52% yield, m.p. 65°-67° C., and that product was reacted with ethylmagnesium to give the required starting material in 49% yield, as a gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05196422 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-978a2252105a4688baa9f58642802d57 |
| Source note | uspto-grants-1993_03 |