HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 3-Benzyloxy-4-(1-adamantyl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Methyl 3-benzyloxy-4-(1-adamantyl)benzoate | HCID 19387981 | — |
| Product | 3-Benzyloxy-4-(1-adamantyl)benzoic acid | HCID 17867034 | — |
Reaction Steps
18 g (63 mM) of the ester obtained in Example 9(a) are treated with benzyl bromide under the conditions described in Example 5(a) to lead, after the same treatment, to 17.5 g (74%) of methyl 3-benzyloxy-4-(1-adamantyl)benzoate. The derivative obtained is then saponified under the conditions described in Example 7(b) to lead, after the same treatment, to 13.6 g (96.6%) of the expected derivative, of melting point 240° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05446059 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-cdab5e5c805e496ca49a6b779eea4dea |
| Source note | uspto-grants-1995_08 |