HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Gentisate → Methyl 5-(2-cyclohexylethoxy)-2-hydroxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Gentisate | HCID 75077 | — |
| Reactant | 2-Cyclohexylethyl 4-methylbenzenesulfonate | HCID 11426070 | — |
| Product | Methyl 5-(2-cyclohexylethoxy)-2-hydroxybenzoate | HCID 19036723 | 43% |
Reaction Steps
Synthesis was carried out in the same manner as in Example 1, except for replacing methyl 2,4-dihydroxybenzoate with methyl 2,5-dihydroxybenzoate and replacing 2-ethylhexyl bromide with 2-cyclohexylethyl p-toluenesulfonate, to obtain methyl 5-(2-cyclohexylethoxy)-2-hydroxybenzoate represented by the following chemical formula (hereinafter referred to as compound 11) as a pale yellow solid in a yield of 43%. The analytical results are shown below. ##STR32##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05646184 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-dde65f479bc54da9b6f090eb6743d7ff |
| Source note | uspto-grants-1997_07 |