HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-(bromomethyl)benzoate → Ethyl 4-(2-ethoxycarbonylbenzyloxy)-alpha-methylphenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-(bromomethyl)benzoate | HCID 11032082 | — |
| Reactant | Ethyl 2-(4-hydroxyphenyl)propanoate | HCID 12785115 | — |
| Product | Ethyl 4-(2-ethoxycarbonylbenzyloxy)-alpha-methylphenylacetate | HCID 54555132 | — |
Reaction Steps
Reaction of ethyl α-methyl-p-hydroxyphenylacetate with ethyl α-bromo-o-toluate by the method described in Example 1b provides ethyl 4-(2-ethoxycarbonylbenzyloxy)-α-methylphenylacetate as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04816591 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-5b9f9d3664864c85a91f6ce9a3c75a8f |
| Source note | uspto-grants-1989_03 |